Introduction

Surgi Plast is a Pakistani medical-device manufacturer associated with disposable injection and infusion products. Public regulatory records place the company at Plot No. 78, Road No. L-4, Industrial Estate, Gadoon Amazai, Khyber Pakhtunkhwa, and identify manufacturing sections for syringes and IV sets.

The company name is particularly relevant to people searching for Surgi Plast syringes, Surgi Plast disposable syringes, Surgi Plast auto-disable syringes, IV sets, and other medical consumables. Pakistan’s Drug Regulatory Authority (DRAP) records also identify Clinic-branded auto-disable syringes manufactured by Surgi Plast, including 2 mL, 3 mL, and 5 mL products under registration number MDMR-000115.

It is important to understand that these products are medical devices rather than medicines. A syringe, IV set, or cannula is equipment used in healthcare delivery; it does not itself represent a drug or treatment. The appropriate device depends on the clinical procedure, medication or fluid being administered, patient requirements, and professional judgment.

This distinction becomes especially important when researching a manufacturer online. A product listing may tell you a size or product name, but purchasing decisions may also require information about the exact model, connector, needle configuration, sterility, expiry date, packaging, batch number, and applicable regulatory documentation.

There is another reason for careful research: Surgi Plast should not be confused with similarly named companies. For example, Relax Surgi Plast is a separate business in Ahmedabad, India, associated with plastic bottles and packaging products.

This guide therefore looks beyond a simple company introduction. It explains what Surgi Plast is, the products associated with it, how syringe specifications work, how to approach safety and batch information, and what healthcare buyers should check before purchasing.

What Is Surgi Plast?

Surgi Plast is a medical-device manufacturer based in Gadoon Amazai, District Swabi, Khyber Pakhtunkhwa, Pakistan. Its manufacturing identity is supported by Pakistan’s regulatory records rather than only by commercial directory listings.

A DRAP establishment-license document lists Surgi Plast at Plot No. 78, Road No. L-4, Industrial Estate, Gadoown Amazai, KPK, with sections for syringes and IV sets and establishment license reference ELM-0030.

Separate DRAP registration records identify Surgi Plast products under the Clinic name. For example, the regulator’s registered medical-device list identifies Clinic Auto Disable Syringes, 2 mL, 3 mL and 5 mL, under registration number MDMR-000115, with Surgi Plast listed as the manufacturer.

The available records provide a stronger way to understand the company than unsupported claims about market size or reputation. Older online material may contain statements about Surgi Plast’s share of the Pakistani market, but such claims should not be treated as current market statistics unless supported by a recent, credible market study.

For buyers, the more useful question is not simply whether a manufacturer is popular. It is whether the specific medical device being purchased can be identified, documented, traced and verified.

That means looking at the product itself, its packaging, registration information where applicable, batch number, expiry date and instructions for use.

Where Is Surgi Plast Located?

The documented manufacturing address is Plot No. 78, Road No. L-4, Industrial Estate, Gadoon Amazai, Khyber Pakhtunkhwa, Pakistan. This address appears in DRAP’s establishment-license records and product-registration information.

Gadoon Amazai is an industrial area in District Swabi, and the presence of Surgi Plast there places the company within Pakistan’s established industrial and medical-device manufacturing landscape.

Verifying the address can be useful when buying medical products because similarly named businesses exist in other countries. A quotation, invoice, certificate or product package should identify the manufacturer clearly enough to distinguish the business from unrelated companies.

For procurement teams, the address is also part of product traceability. If a supplier provides documentation under a slightly different company name or address, the discrepancy should be clarified rather than ignored.

What Does the CLINIC Brand Represent?

Clinic appears in Pakistani regulatory records as a product name associated with Surgi Plast. DRAP lists Clinic Auto Disable Syringes in 2 mL, 3 mL and 5 mL sizes under MDMR-000115.

The important point is that a brand name does not replace the technical specification. Two products carrying the same general brand may have different capacities, needle configurations, packaging or intended applications.

Therefore, when a healthcare facility orders Clinic or another Surgi Plast product, the purchase request should identify the exact item rather than simply saying “Clinic syringe.”

What Products Does Surgi Plast Make?

Available Pakistani regulatory information connects Surgi Plast with several categories of medical devices, particularly syringes and IV sets. Its registered products include Clinic disposable and auto-disable syringes.

Product information should always be checked against current manufacturer documentation because catalogues can change and different models can have different specifications.

Surgi Plast Disposable Syringes

A disposable syringe is a medical device designed to draw up or deliver fluids. It generally consists of a barrel, plunger and connection point, with some configurations supplied with a needle.

The capacity may vary considerably. A small syringe can be appropriate for applications requiring precise measurement of a relatively small volume, while larger syringes can be designed for different clinical or procedural requirements.

A key safety principle is that a single-use syringe should not be reused between patients. The CDC states that healthcare providers should use a syringe once and then discard it, and that changing the needle does not make a used syringe safe for another patient.

For purchasing purposes, therefore, the brand is only one part of the specification. Buyers should confirm:

• Syringe capacity
• Needle size, if included
• Needle attachment
• Connector type
• Sterility status
• Packaging
• Intended use
• Batch or lot number
• Expiry information

This prevents a common purchasing error: assuming that all syringes from one manufacturer have identical characteristics.

Surgi Plast Auto-Disable Syringes

An auto-disable syringe contains a mechanism intended to prevent reuse. This is particularly relevant to immunization programs, where preventing syringe reuse is an important part of injection safety.

WHO states that auto-disable syringes are the type of single-use injection device it strongly recommends for vaccine administration and notes that these devices are designed so they cannot be reused in the normal manner.

DRAP’s records identify Surgi Plast’s Clinic Auto Disable Syringes in 2 mL, 3 mL and 5 mL configurations under MDMR-000115.

However, the term auto-disable should not be interpreted as meaning that every safety feature is automatically present. An auto-disable mechanism concerns reuse prevention; it does not necessarily mean the needle retracts into the syringe or becomes completely shielded after use.

When purchasing an auto-disable syringe, the exact model and mechanism should therefore be confirmed from the manufacturer’s documentation.

Surgi Plast IV Sets

An IV set is an administration system used to deliver fluids or medications through intravenous access. Depending on the design, an infusion set may include tubing, connectors, a drip chamber and other components.

Compatibility is important because an IV set is not an isolated device. It must connect appropriately with the relevant IV access equipment and fluid container or administration system.

CDC guidance emphasizes that fluid infusion and administration sets should be used for one patient and disposed of appropriately after use.

For purchasing, a clinic should therefore check the exact IV-set configuration rather than relying only on the product category. Relevant questions may include connector type, tubing configuration, sterile packaging, intended application and compatibility requirements.

Surgi Plast Scalp Vein Sets

Scalp vein sets, sometimes called butterfly sets, combine a small needle with flexible tubing and wings that help with handling and stabilization.

Despite the word “scalp” in the name, the terminology does not mean that the product is limited to one specific body location. These devices are used in healthcare settings for particular forms of vascular access, with the exact use determined by trained professionals.

A buyer should check the needle gauge, needle length, tubing, connection type and packaging. These details can vary between products.

Patients should not select a scalp vein set independently for treatment. The healthcare professional performing the procedure should determine the appropriate equipment based on the clinical situation.

Surgi Plast IV Cannulas

An IV cannula is a device used to establish vascular access so that fluids or medicines can be administered intravenously.

Cannulas are commonly described using gauge, such as 18G, 20G, 22G or 24G. The gauge number describes the size of the device, but the relationship between gauge and physical dimensions is not the same as syringe capacity.

Regulatory documentation from Pakistan also shows Surgi Plast associated with IV-cannula-related regulatory activity, illustrating that cannula specifications should be treated separately from syringe specifications.

The correct cannula should be selected according to the procedure and clinical requirements by qualified healthcare personnel.

Understanding Surgi Plast Syringe Specifications

A syringe can appear simple, but several technical terms can affect whether one configuration is appropriate for a particular application.

Syringe Capacity: 1 mL, 3 mL, 5 mL, 10 mL and 20 mL

Syringe capacity describes the approximate maximum volume the barrel is designed to hold. mL means millilitre, while cc is commonly used as an equivalent volume measurement in medical contexts.

Capacity should not be confused with the prescribed dose.

For example, a 5 mL syringe does not mean that a patient should receive 5 mL of medication. It only describes the syringe’s capacity. The actual volume administered depends on the medication, prescription, procedure and professional instructions.

Smaller syringes can offer useful measurement characteristics for small volumes, while larger syringes may be selected when more fluid needs to be handled. The correct choice depends on the procedure rather than the brand alone.

DRAP’s records demonstrate why exact identification matters: Surgi Plast has registrations covering different syringe types and capacities, including Clinic auto-disable syringes and other Clinic disposable syringe configurations.

A purchasing request should therefore identify the desired size and configuration rather than simply requesting “Surgi Plast syringes.”

Needle Gauge and Length

Needle specifications answer a different question from syringe capacity.

A notation such as 23G × 1 inch contains two pieces of information. The gauge describes needle diameter, while the inch measurement describes its length.

A 24G needle is not simply a “24 mL needle.” Gauge is a needle-dimension system, while mL refers to volume.

This distinction is useful because two syringes may have the same capacity while being supplied with different needles. Likewise, a syringe can sometimes be supplied without a permanently attached needle, depending on its design.

For example, WHO’s published information for a different Pakistani manufacturer’s 5 mL auto-disable syringe identifies a 23G × 1-inch needle configuration, illustrating how capacity and needle specifications are listed as separate characteristics.

For Surgi Plast products, buyers should use the actual product documentation rather than assuming a needle configuration from the syringe size.

Luer Lock vs. Luer Slip

The Luer system is a standardized connection approach used in many medical devices.

A Luer-lock connection uses a locking mechanism to secure compatible components. A Luer-slip connection relies on a friction fit.

The distinction matters because the connector affects which compatible component can be attached and how that connection is secured.

However, Luer lock does not mean auto-disable. These are completely different characteristics:

• Luer lock: describes the connection mechanism.
• Luer slip: describes a friction-fit connection.
• Auto-disable: describes a reuse-prevention mechanism.
• Sharps protection: concerns protection from needle injuries.

Keeping these terms separate makes product comparison much easier.

Auto-Disable vs. Sharps Protection

Auto-disable technology is intended primarily to prevent reuse. Sharps-protection technology is intended to reduce the risk associated with handling an exposed needle.

These features can coexist, but one should not automatically be assumed from the other.

WHO’s information on auto-disable syringes focuses specifically on preventing reuse and reducing the risk of person-to-person transmission associated with reused injection equipment.

This distinction is important for buyers because a product description that says “auto-disable” does not necessarily mean that it has a retractable needle or a particular sharps shield.

Always check the actual device design and instructions.

Surgi Plast Safety and Regulatory Information

Medical-device safety is best evaluated at the product and batch level.

A manufacturer can have multiple products, sizes and production batches. A regulatory notice concerning one specific device or batch should not automatically be generalized to every product made by the company.

Pakistan’s DRAP database provides useful evidence for identifying Surgi Plast products. For example, it records Clinic Auto Disable Syringes 2 mL, 3 mL and 5 mL under MDMR-000115.

Checking Surgi Plast Batch Numbers

A batch or lot number allows a specific group of products to be traced.

When receiving medical supplies, a healthcare facility should record:

1. Product name
2. Product size
3. Batch/lot number
4. Expiry date
5. Quantity
6. Supplier
7. Invoice information
8. Date received

If a regulatory notice later identifies a particular batch, this record makes it much easier to determine whether the facility has affected stock.

If stock appears to match an official safety notice, it should be handled according to the regulator’s instructions and the facility’s established recall procedure. Users should not independently decide to continue using a potentially affected medical device.

Understanding Recall or Substandard Product Notices

In 2026, public reporting of Pakistani regulatory action identified Clinic Auto Disable Syringe 3 mL/cc, registration number MDMR-000115, with batches 3-01C-26 and 3-01B-26 associated with a substandard finding concerning the auto-disable/reuse-prevention function.

This information should be interpreted narrowly.

It identifies specific batches of a particular product. It does not, by itself, establish that every Surgi Plast product is defective or that every syringe manufactured by the company is affected.

That distinction is essential when discussing medical-device safety.

If a facility has potentially affected stock, the appropriate response is to identify the exact product and batch and follow current instructions from DRAP and the responsible procurement or clinical authority.

Why Product Registration Information Matters

Registration numbers help distinguish one medical device from another.

For example, DRAP lists Surgi Plast’s Clinic Auto Disable Syringes under MDMR-000115.

A registration number should be matched with the actual product name and manufacturer rather than copied from an unrelated document.

Buyers should also avoid treating an old certificate image, marketplace listing or directory entry as proof of current regulatory status. Current information from the relevant authority is more useful for a present purchasing decision.

Sterility and Packaging of Surgi Plast Medical Devices

Sterility is one of the most important considerations for sterile injection and infusion equipment.

What Does EO or Ethylene Oxide Sterilization Mean?

Ethylene oxide (EO) is a sterilization method widely used for certain medical devices. The FDA explains that EO can be useful for devices made from materials such as plastics and for products with complex structures or packaging that may not be suitable for other sterilization methods.

The presence of EO sterilization information on packaging means the manufacturer has used a particular sterilization process. It does not mean that users should attempt to sterilize a disposable device at home.

A healthcare facility should follow the manufacturer’s instructions for use and the applicable infection-control procedures.

Why Intact Packaging Matters

Sterility depends not only on the manufacturing process but also on the integrity of the sterile barrier.

A package that is torn, punctured, opened or otherwise compromised may no longer provide the expected protection.

When receiving Surgi Plast medical supplies, procurement or clinical staff should inspect:

• Outer packaging
• Individual sterile packaging
• Seals
• Product condition
• Expiry date
• Batch number
• Sterility information

If packaging integrity is questionable, the product should not simply be treated as sterile because the label says it was sterilized.

Single-Use Medical Devices

Disposable syringes and many related injection devices are designed for single use.

CDC guidance is explicit that needles and syringes should not be reused for another patient. It also notes that changing a needle does not make a used syringe safe for another patient.

This is important because contamination can occur inside the syringe even when the needle has been replaced.

The same principle applies to infusion equipment: CDC guidance recommends using fluid infusion and administration sets for one patient and disposing of them appropriately after use.

Surgi Plast and Similarly Named Companies

Online searches for “Surgi Plast” can produce results from different businesses.

Surgi Plast Pakistan

The Pakistani manufacturer is documented in DRAP records at Gadoon Amazai, District Swabi, Khyber Pakhtunkhwa. Its regulatory record includes syringes and IV-set manufacturing sections, while registered products include Clinic-branded syringes.

Relax Surgi Plast, India

Relax Surgi Plast is a different business based in Ahmedabad, Gujarat, India. Available business information describes it as a manufacturer/supplier of plastic products including bottles and pesticide packaging.

The similar name can easily cause search confusion, particularly when someone searches for product information without checking the country or business address.

These companies should therefore not be treated as the same manufacturer.

How to Avoid Confusing the Two Businesses

Before placing an order, compare:

• Complete company name
• Country
• Manufacturing address
• Product category
• Product name
• Packaging
• Registration information
• Invoice details
• Supplier documentation

A product photograph alone is not sufficient to establish the identity of the manufacturer.

How to Choose Surgi Plast Products for Healthcare Purchasing

Purchasing medical devices requires more than comparing prices.

Confirm the Exact Product

Start with the exact product name and configuration.

For a syringe, this may include:

• Capacity
• Needle size
• Needle length
• Connector
• Fixed or detachable needle
• Disposable or auto-disable design
• Sterility status

For an IV set or cannula, additional specifications may apply.

Check Batch, Expiry and Packaging

Before accepting stock, check the batch number and expiry date. Inspect the packaging for damage and confirm that sterile barriers are intact where applicable.

This simple receiving process can make future product tracking considerably easier.

Request Product Documentation

Healthcare buyers can request appropriate documentation such as:

• Product specification sheet
• Instructions for use
• Applicable registration information
• Quality documentation
• Batch information
• Sterility information
• Supplier invoice

The documentation should correspond to the exact product being supplied.

Compare Complete Quotations

The lowest unit price does not necessarily represent the lowest total purchasing cost.

A quotation should ideally identify:

• Price
• Pack quantity
• Product configuration
• Delivery cost
• Lead time
• Taxes or other applicable charges
• Replacement terms
• Return procedures

Comparing complete quotations prevents a buyer from accidentally comparing different products or pack sizes.

Surgi Plast for Clinics, Hospitals and Medical Suppliers

For healthcare organizations, product identification is only the beginning. Inventory traceability is equally important.

Why Product Traceability Matters

A batch number creates a connection between physical stock and purchasing records.

If a safety notice is issued later, the organization can search its inventory records and determine whether the affected product entered the facility.

This is especially useful for medical devices because a regulatory notice may identify a specific model, registration number and batch rather than an entire manufacturer.

Creating a Simple Medical-Supply Receiving Record

A useful receiving record can include:

Information	What to record
Supplier	Company or distributor name
Product	Exact product name
Quantity	Number of units/cartons
Batch	Lot or batch number
Expiry	Expiry date
Invoice	Invoice/reference number
Date	Date received
Location	Storage area

This does not need to be complicated. Even a properly maintained spreadsheet or inventory system can improve traceability.

Stock Rotation and Expiry Management

Healthcare facilities should regularly review stock and use appropriate inventory-rotation procedures.

Products approaching expiry should be identified according to the facility’s inventory policy, while expired, damaged or questionable products should be separated from usable stock.

If a regulator identifies a particular batch as affected, the facility should be able to locate that batch quickly rather than searching through every carton.

What Patients Should Know About Surgi Plast Syringes

Patients do not need to memorize syringe specifications to ask sensible questions.

Before an injection or similar procedure, a patient can reasonably ask whether the equipment is new and whether the packaging is intact.

The most important safety principle is that needles and syringes should not be reused between patients. CDC guidance states that providers should use a new sterile syringe and needle for each patient and discard them after use.

Patients also should not attempt to select their own syringe based solely on capacity. A syringe’s size does not determine the appropriate medication dose, injection technique or clinical application.

Those decisions belong to the qualified healthcare professional responsible for treatment.

If someone is specifically concerned about a recalled or substandard device, the useful information is the manufacturer, product name, size, registration/reference number and batch number. A manufacturer name by itself may not be enough to determine whether a particular item is affected.

Safe Disposal of Surgi Plast Syringes and Needles

Used injection devices should be treated as sharps.

Why Used Syringes Are Sharps

Needles can cause puncture injuries after use. They may also be contaminated with blood or other biological material.

CDC identifies improper handling and disposal of needles and syringes as an injection-safety concern.

For this reason, used devices should not simply be left on a work surface or placed loose into ordinary waste.

Sharps Containers

Appropriate sharps containers are designed to reduce the risk of puncture injuries and exposure.

WHO guidance on injection safety also highlights the importance of safety boxes or puncture-proof containers for used syringes and needles.

Healthcare facilities should follow their local waste-management requirements and established infection-control procedures.

Auto-Disable Does Not Mean Risk-Free Disposal

An auto-disable syringe is designed to prevent reuse, but the device may still contain a needle or other sharp component.

Therefore, reuse prevention and sharps disposal are separate safety issues.

Even after the auto-disable mechanism has operated, the used device should be handled and discarded through the appropriate sharps-waste process.

Advantages of Understanding Surgi Plast Product Specifications

Better Purchasing Accuracy

Knowing the exact capacity, needle configuration and connector helps a buyer order the intended product rather than a vaguely similar item.

Better Inventory Traceability

Recording product and batch information makes future checks much easier.

Better Communication With Suppliers

A precise request produces a more useful quotation. Instead of asking for “Surgi Plast syringes,” a buyer can specify the exact product, size and configuration required.

Better Safety Awareness

Understanding terms such as sterile, single-use, auto-disable, batch and expiry helps users recognize which information matters when receiving medical devices.

The goal is not to judge a manufacturer based on one label or one online review. It is to connect the actual product with reliable documentation and current regulatory information.

Common Mistakes to Avoid When Buying Surgi Plast Products

Several mistakes can make medical-device purchasing less reliable:

1. Buying only by brand name without confirming the product configuration.
2. Ignoring batch numbers that are essential for traceability.
3. Comparing prices without checking pack sizes.
4. Assuming every syringe comes with the same needle.
5. Confusing Luer lock with auto-disable technology.
6. Accepting damaged sterile packaging.
7. Confusing Surgi Plast Pakistan with Relax Surgi Plast India.
8. Relying on outdated online catalogues.
9. Reusing single-use injection equipment.
10. Ignoring current regulatory notices.

These mistakes are avoidable when purchasing teams use a structured checklist.

How to Verify Surgi Plast Products Before Purchase

Before ordering or accepting Surgi Plast medical supplies, work through this checklist:

1. Confirm the manufacturer name.
2. Confirm the manufacturing address.
3. Identify the exact product.
4. Check the capacity or size.
5. Check needle and connector specifications.
6. Verify the batch or lot number.
7. Check the expiry date.
8. Inspect the packaging.
9. Request current product documentation.
10. Check relevant regulatory information.
11. Obtain a dated quotation.
12. Keep supplier and invoice records for traceability.

This process is useful because it shifts the purchasing decision from a general brand-based assessment to a product-specific verification process.

For medical devices, that distinction can be significant. A product name identifies what you are looking at, but specifications, documentation and batch information tell you more about the particular item in front of you.

Frequently Asked Questions About Surgi Plast

What is Surgi Plast?

Surgi Plast is a Pakistani medical-device manufacturer associated with syringes and IV-related products. DRAP records identify its manufacturing location in Gadoon Amazai, Khyber Pakhtunkhwa, and list registered Clinic-branded syringe products.

Where is Surgi Plast located?

Surgi Plast is documented at Plot No. 78, Road No. L-4, Industrial Estate, Gadoon Amazai, District Swabi, Khyber Pakhtunkhwa, Pakistan.

What products does Surgi Plast manufacture?

Regulatory records associate the company with syringe and IV-set manufacturing. Its registered products include Clinic auto-disable syringes, while other available information associates it with disposable syringes and related medical consumables.

What is the CLINIC brand?

Clinic is a product name associated with Surgi Plast’s medical devices. DRAP records identify Clinic Auto Disable Syringes manufactured by Surgi Plast under MDMR-000115.

Does Surgi Plast make auto-disable syringes?

Yes. DRAP’s registered-device list identifies Clinic Auto Disable Syringes in 2 mL, 3 mL and 5 mL configurations under MDMR-000115.

Can disposable Surgi Plast syringes be reused?

Single-use syringes should not be reused between patients. CDC guidance specifically states that changing the needle does not make a used syringe safe for another patient.

How can I check a Surgi Plast batch?

Find the batch or lot number on the product packaging and compare it with current information from DRAP or other relevant regulatory sources. If the batch is identified in a safety notice, follow the regulator’s instructions and contact the supplier or responsible healthcare authority.

Is Relax Surgi Plast the same as Surgi Plast Pakistan?

No. The available information identifies Relax Surgi Plast as a separate business in Ahmedabad, India, associated with plastic packaging products.

What should I check before buying Surgi Plast products?

Check the exact product name, size, needle or connector configuration, batch number, expiry date, packaging, applicable registration information, current safety notices, documentation and supplier details.

Conclusion: Understanding Surgi Plast Before Buying or Using Its Products

Surgi Plast is a Pakistan-based medical-device manufacturer documented in regulatory records at Gadoon Amazai, District Swabi. Its regulatory profile includes syringe and IV-set manufacturing sections, while Clinic-branded auto-disable syringes are among the products registered under its name.

For anyone researching Surgi Plast Pakistan, the most useful approach is to focus on individual products rather than making broad assumptions about the entire company. Disposable syringes, auto-disable syringes, IV sets and cannulas each have different technical requirements.

Buyers should pay particular attention to capacity, needle specifications, connectors, sterility, packaging, expiry dates, batch numbers and applicable regulatory documentation. These details provide much more practical information than a brand name alone.

The 2026 regulatory information concerning specific Clinic auto-disable syringe batches also demonstrates why batch-level verification matters. Public reporting identified batches 3-01C-26 and 3-01B-26 in connection with a substandard finding concerning the auto-disable function. That information should not be generalized to every Surgi Plast product or every batch.

Finally, remember that Surgi Plast Pakistan and Relax Surgi Plast in India are separate businesses. Checking the full company name, address and product documentation can prevent unnecessary confusion.

For a healthcare facility, the practical takeaway is straightforward: identify the exact device, verify its documentation, check the batch and expiry information, inspect the packaging, and consult current regulatory information before purchasing or using medical supplies.