Surgi Plast: A Complete Guide to the Pakistani Medical Device Manufacturer, Products, and Safety Standards
Introduction
The healthcare industry depends on reliable medical equipment to support doctors, nurses, hospitals, clinics, and patients. From disposable syringes to intravenous equipment, medical devices play an important role in everyday healthcare services. One company associated with this industry in Pakistan is Surgi Plast, a medical-device manufacturer based in Gadoon Amazai, District Swabi, Khyber Pakhtunkhwa.
Surgi Plast is known for its association with disposable medical products, including syringes and intravenous (IV) equipment. Its products are connected with the CLINIC brand, which appears in Pakistani medical-device registration records. The company is particularly relevant to people researching local medical manufacturers, healthcare supplies, and disposable injection equipment.
However, understanding a medical-device manufacturer involves more than knowing its location and product range. Buyers and healthcare professionals also need to understand product specifications, regulatory requirements, manufacturing standards, and safety information.
This article explores Surgi Plast, its background, products, role in the Pakistani healthcare industry, and important considerations when evaluating its medical equipment.
What Is Surgi Plast?
Surgi Plast is a Pakistani medical-device manufacturing company located at Plot No. 78, Road No. L-4, Industrial Estate, Gadoon Amazai, District Swabi, Khyber Pakhtunkhwa.
The company is associated with manufacturing disposable syringes and IV-related medical equipment. Its manufacturing activities are also reflected in records published by the Drug Regulatory Authority of Pakistan (DRAP).
According to publicly available regulatory information, Surgi Plast is listed under establishment licence number ELM-0030. Its documented manufacturing sections include syringes and IV sets.
The company operates in an important segment of the healthcare supply chain. Medical facilities require dependable supplies of disposable equipment to perform routine procedures, administer medications, and deliver fluids to patients.
Surgi Plast is therefore a relevant name for people interested in Pakistan’s medical-device manufacturing sector.
It is important, however, to distinguish verified company information from unsupported marketing claims. Details such as production capacity, market share, and overall product quality should be assessed using reliable and current documentation rather than assumptions.
Background and Business Location
Surgi Plast is associated with the Gadoon Amazai Industrial Estate in Khyber Pakhtunkhwa. This industrial location is relevant because the manufacturing of medical devices requires specialised facilities, production processes, packaging systems, and quality-control procedures.
The company’s listed address helps healthcare buyers, distributors, and business researchers identify the correct manufacturer when reviewing product documentation.
Its establishment licence information also provides a useful starting point for understanding its regulated manufacturing activities.
The development of domestic medical-device manufacturing is important for Pakistan. Hospitals and clinics need a continuous supply of healthcare consumables, and local manufacturers can contribute to the availability of these essential products.
Nevertheless, manufacturing locally does not automatically establish that every product meets the required safety standards. Individual products must be assessed according to their registration, labelling, manufacturing controls, and applicable regulatory requirements.
Products Associated With Surgi Plast
Medical-device manufacturers generally produce different equipment for specific healthcare applications. Surgi Plast is associated with several types of disposable medical products.
1. Disposable Syringes
Disposable syringes are among the main products associated with Surgi Plast. They are commonly used in hospitals, clinics, laboratories, and other healthcare environments.
A disposable syringe generally consists of a transparent barrel, a plunger, and a tip that connects to a needle or another compatible medical component.
Different syringe capacities are designed for different procedures. For example, smaller syringes may be used for administering measured medication doses, while larger sizes can be suitable for procedures requiring greater fluid capacity.
Healthcare professionals must select the correct syringe according to the prescribed medication, procedure, and manufacturer’s instructions.
2. Auto-Disable Syringes
Auto-disable syringes are designed to prevent reuse after a single injection. They contain a mechanism that makes the syringe permanently inoperable after use.
These devices are particularly important in vaccination programmes and public health initiatives because they help reduce the risk of unsafe syringe reuse.
DRAP records identify a Clinic Auto Disable Syringe manufactured by Surgi Plast under medical-device registration number MDMR-000115.
However, an important distinction must be made between product design and actual performance. An auto-disable syringe must successfully pass the required functional tests to demonstrate that its reuse-prevention mechanism works correctly.
3. Intravenous (IV) Sets
IV sets are medical devices used to deliver fluids and certain prescribed medications directly into a patient’s bloodstream through an established intravenous access point.
A typical IV set includes tubing, a drip chamber, connectors, and other components needed for controlled fluid administration.
These products are commonly used in hospitals and medical centres. Their proper selection and use depend on the treatment requirements and the healthcare professional’s instructions.
DRAP’s establishment-licence records identify an IV-set manufacturing section associated with Surgi Plast. dra.gov.pk
4. Other Injection-Related Equipment
Medical-device catalogues and business listings associate Surgi Plast with different injection and infusion supplies.
When researching these products, buyers should distinguish between general company listings and officially registered devices. A product appearing in a catalogue does not necessarily establish its current registration status or availability.
Checking the exact product name, model, and regulatory documentation is therefore essential.
Understanding the CLINIC Brand
CLINIC is a product brand associated with Surgi Plast. It appears in Pakistani regulatory documentation for medical devices manufactured by the company.
One documented example is the Clinic Auto Disable Syringe, which has registration number MDMR-000115.
Brand identification is useful for hospitals, distributors, and healthcare professionals because it helps them distinguish products from different manufacturers.
However, a familiar brand name should never replace proper product inspection. Medical-device safety depends on factors such as manufacturing quality, sterility, packaging, labelling, storage, and batch-specific performance.
Healthcare facilities should also maintain purchasing records so that individual products can be traced if a regulatory notice is issued.
Surgi Plast and Pakistan’s Healthcare Industry
Pakistan’s healthcare system relies on a combination of imported and locally manufactured medical equipment. Domestic manufacturers contribute to the supply of products that hospitals and clinics use every day.
Surgi Plast operates within this important manufacturing sector by being associated with syringes and IV sets.
Local production can offer several potential advantages:
- Greater availability of commonly required medical consumables.
- Opportunities to develop domestic manufacturing expertise.
- Support for local industrial employment.
- Reduced dependence on certain imported products.
- Opportunities for distribution through domestic healthcare suppliers.
Nevertheless, these advantages depend on consistent manufacturing quality and effective regulatory oversight.
Medical devices are directly involved in patient care. Consequently, manufacturers must pay particular attention to sterility, material quality, accurate labelling, packaging integrity, and product performance.
For hospitals and distributors, choosing medical supplies should always involve a careful assessment of regulatory status and product-specific documentation.
DRAP Registration and Regulatory Oversight
The Drug Regulatory Authority of Pakistan plays an important role in regulating medical devices and protecting public health.
Its responsibilities include overseeing medical-device manufacturers, maintaining regulatory information, and issuing safety alerts when products are identified as defective or non-compliant.
According to DRAP’s establishment-licence list published up to July 21, 2025, Surgi Plast appears under establishment licence ELM-0030, with approved sections for syringes and IV sets. dra.gov.pk
It is important to understand that an establishment licence and an individual medical-device registration are not the same thing.
- Establishment licence: Identifies the licensed manufacturing establishment and its approved manufacturing activities.
- Device registration: Identifies a particular medical device that has been registered under the applicable regulatory framework.
- Batch number: Identifies a particular production batch and helps with traceability.
- Expiry date: Indicates the manufacturer’s stated period of product validity under specified storage conditions.
Checking these details helps healthcare buyers make more informed purchasing decisions.
Important Surgi Plast Safety Alerts in 2026
One of the most important aspects of researching Surgi Plast is understanding the safety notices published by DRAP in 2026.
These notices concern specific batches of CLINIC-branded syringes. They should be taken seriously by distributors, pharmacists, healthcare professionals, and consumers.
Auto-Disable Syringe Recall
On June 8, 2026, DRAP published Recall Alert No. N° I/S/06-26-34 concerning a Clinic Auto Disable Syringe 3 mL manufactured by Surgi Plast.
The affected batch number was 3-01B-26.
According to the regulator, laboratory testing identified a failure in the self-destructive performance or auto-disable mechanism. This meant that the device did not meet the required reuse-prevention performance.
DRAP explained that defective auto-disable syringes could create risks associated with reuse, including the transmission of blood-borne infections such as hepatitis B, hepatitis C, and HIV.
The regulator instructed pharmacies and medical stores to stop supplying the affected batch, quarantine remaining stock, and return it to suppliers. Healthcare facilities and consumers possessing the affected batch were also advised to stop using it. Drug Regulatory Authority of Pakistan
Disposable Syringe Safety Alert
Another important notice appeared in DRAP Recall Alert No. N° I/S/10-26-42.
The alert concerned CLINIC Disposable Syringes measuring 20 mL, manufactured by Surgi Plast.
The affected batch number was 20-01G-25.
According to DRAP, laboratory testing identified two problems:
- The sample failed sterility testing.
- The product label mentioned two different needle gauges, creating a misbranding concern.
The regulator explained that non-sterile syringes could introduce microorganisms into patients, potentially causing infections. Conflicting needle-gauge information could also lead to incorrect product selection.
DRAP instructed distributors and pharmacies to stop supplying the affected batch. Healthcare facilities and consumers possessing it were advised to discontinue use and contact their suppliers for return or replacement. Drug Regulatory Authority of Pakistan
What Do These Alerts Mean for Customers?
These notices concern identified products and batch numbers. They do not establish that every product manufactured by Surgi Plast is affected.
However, they demonstrate why checking product-specific safety information is essential.
Healthcare facilities should verify the batch number, packaging, expiry date, and current regulatory status before accepting or using medical supplies.
If a product matches an affected batch, it should not be used.
Quality Control and Product Safety Considerations
Quality control is one of the most important responsibilities in medical-device manufacturing. Even a small manufacturing defect can affect patient safety.
For syringe manufacturers, quality assurance should cover several important areas.
Sterility testing: Disposable medical devices intended for sterile use must meet applicable sterility requirements. Proper sterilization and packaging help protect patients from contamination.
Material inspection: Medical-grade materials must be suitable for their intended applications. Manufacturers should maintain appropriate controls over raw materials and production processes.
Accurate labelling: Product packaging should clearly identify the syringe capacity, needle specifications, manufacturer, batch number, and expiry date where applicable.
Functional testing: Special features, including auto-disable mechanisms, must work as intended.
Packaging integrity: Medical devices should remain protected from contamination and physical damage during transportation and storage.
These measures are important for every medical-device manufacturer, including Surgi Plast.
What Buyers Should Check Before Purchasing Surgi Plast Products
Hospitals, clinics, pharmacies, and medical distributors should follow a systematic purchasing process.
Here are some important considerations:
- Verify the manufacturer’s complete identity and address.
- Check the medical-device registration information.
- Confirm the exact product name and specifications.
- Examine the batch or lot number.
- Check the expiry date.
- Inspect the packaging for damage or tampering.
- Confirm that the sterile packaging is properly sealed.
- Review current DRAP recall and safety notices.
- Purchase through reliable and traceable suppliers.
- Maintain invoices and product documentation.
These precautions help healthcare organisations identify potentially defective products before they enter clinical use.
The Importance of Disposable Medical Devices
Disposable medical devices have transformed modern healthcare by supporting safer and more organised medical procedures.
Single-use syringes, for example, help reduce the risk of cross-contamination when used correctly and discarded after one procedure.
Similarly, IV sets support the administration of fluids and prescribed medications in different healthcare settings.
However, disposable equipment is only effective when it meets the necessary safety requirements. Correct storage, proper handling, and appropriate disposal are equally important.
Healthcare professionals should always follow established infection-control procedures and the manufacturer’s instructions.
Future Opportunities for Surgi Plast
Pakistan’s medical-device industry has opportunities to grow through technological development, improved quality systems, and stronger regulatory compliance.
Companies such as Surgi Plast operate in a sector where product reliability is essential. Improving manufacturing processes, investing in laboratory testing, strengthening documentation, and maintaining transparent communication with healthcare customers can help manufacturers build confidence.
There is also growing importance attached to traceability. Digital batch records and better distribution monitoring can make it easier to identify products affected by safety notices.
Another opportunity involves developing more consistent quality-management practices. Medical-device manufacturers must continually evaluate their processes rather than relying solely on historical performance.
For Surgi Plast, maintaining regulatory compliance and addressing the concerns highlighted in the 2026 safety alerts are particularly important considerations for its future reputation.
Frequently Asked Questions About Surgi Plast
1. What is Surgi Plast?
Surgi Plast is a Pakistani medical-device manufacturer associated with disposable syringes and intravenous medical equipment.
2. Where is Surgi Plast located?
The company is listed at Plot No. 78, Road No. L-4, Industrial Estate, Gadoon Amazai, District Swabi, Khyber Pakhtunkhwa, Pakistan.
3. What products are associated with Surgi Plast?
Its documented manufacturing activities include syringes and IV sets. Its products are also associated with the CLINIC brand.
4. What is the CLINIC brand?
CLINIC is a medical-device brand associated with Surgi Plast. DRAP records identify Clinic Auto Disable Syringes under registration number MDMR-000115.
5. Is Surgi Plast listed with DRAP?
Yes. DRAP’s published establishment-licence list identifies Surgi Plast under licence number ELM-0030, with syringe and IV-set manufacturing sections.
6. Were Surgi Plast products recalled in 2026?
Yes. DRAP issued safety notices concerning specific batches of CLINIC 3 mL auto-disable syringes and 20 mL disposable syringes in 2026.
7. Why was the 3 mL syringe batch recalled?
The affected batch, 3-01B-26, failed the self-destructive performance or auto-disable test, which is designed to prevent syringe reuse.
8. Why was the 20 mL syringe batch declared substandard?
The affected batch, 20-01G-25, failed sterility testing and had incorrect labelling because two different needle gauges were mentioned.
9. Are all Surgi Plast products affected by these recalls?
The published alerts identify specific products and batches. They do not establish that every product manufactured by the company is affected. Buyers should check current regulatory notices before purchasing or using individual products.
10. What should someone do if they have an affected syringe?
Stop using the affected product, separate it from usable stock, and contact the supplier or manufacturer for return or replacement. Healthcare facilities should follow DRAP’s instructions.
Conclusion
Surgi Plast is a Pakistani medical-device manufacturer associated with disposable syringes, auto-disable syringes, and IV-related equipment. Located in Gadoon Amazai, Swabi, the company is part of Pakistan’s domestic medical manufacturing industry.
Its connection with the CLINIC brand and its appearance in DRAP establishment and device-registration records make it a relevant name for people researching local healthcare manufacturers.
However, the 2026 DRAP safety alerts highlight an important issue: medical-device quality must always be evaluated through reliable testing, accurate labelling, proper sterility, and batch-specific regulatory information.
For healthcare professionals, distributors, and buyers, the best approach is to verify each product before use instead of relying exclusively on a manufacturer’s name or brand reputation.
Ultimately, the future of Surgi Plast depends not only on manufacturing medical equipment but also on maintaining consistent quality, regulatory compliance, transparency, and patient safety.
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