A syringe is a small part of a hospital’s supplies, but its quality matters every time it is used. The same applies to the equipment that carries fluids to a patient. These everyday items help explain the work of Surgi Plast, a medical-device manufacturer based in Pakistan.
The company is associated with disposable injection and infusion supplies sold under the CLINIC brand. Its name appears in Pakistan’s official medical-device registration records alongside several syringe types and other clinical products. Those records offer a useful picture of the business, while safety notices provide further information that buyers should understand.
What Is Surgi Plast?
Surgi Plast makes medical disposables: equipment intended for use in healthcare procedures. Its website groups products under syringes, IV sets and scalp vein sets. The catalogue includes both conventional disposable syringes and auto-disable models.
These products belong to the equipment side of healthcare. A syringe helps deliver a substance; it is separate from the medicine inside it. Understanding that distinction makes the company’s role easier to follow.
A useful company profile therefore starts with the actual devices. Product names, sizes, instructions and registration details tell readers more than broad claims about being a leading manufacturer.
Where Is the Company Based?
The company lists its address as Plot 78, Road L4, Industrial Estate Gadoon Amazai, District Swabi, Khyber Pakhtunkhwa, Pakistan. This places its operations in the Gadoon Amazai industrial area.
For someone checking a supplier’s paperwork, the manufacturing address is a helpful reference. A company name alone may leave room for confusion, especially when businesses have similar names.
The address should be checked alongside the manufacturer details printed on the product and supplied in supporting documents. Together, these details help establish which business made the item being offered.
Understanding the CLINIC Product Range
DRAP’s published registration list identifies Clinic Auto Disable Syringes in 2 mL, 3 mL and 5 mL sizes under registration number MDMR-000115. It also records Clinic disposable syringes, an IV infusion set and a blood transfusion set manufactured by Surgi Plast.
The range covers several product categories, so the brand name should be the beginning of a product check. Buyers still need the exact model and specification.
For example, an order described only as “Clinic syringes” leaves important questions unanswered. The required capacity, needle details, connection type and safety features should all be clear before an order is accepted.
Disposable and Auto-Disable Syringes
The terms disposable and auto-disable describe related but different features. A disposable syringe is intended for single use. An auto-disable syringe includes a mechanism designed to prevent it from being used again after that use.
The World Health Organization explains that reuse-prevention designs can work in different ways. Some block movement of the plunger, while others use a component that breaks when someone attempts reuse. The exact design depends on the device.
This distinction matters when comparing products. A single-use label describes the intended use, while an auto-disable feature adds a physical barrier against reuse.
Buyers should also check whether a product offers protection against accidental needle injuries. Reuse prevention and needle-injury protection are separate features, and one should never be assumed from the other.
What the 5 mL Product Page Says
Surgi Plast’s website describes its 5 mL auto-disable syringe as a single-use product supplied with a needle. The page lists a 23/24G × 1-inch needle specification and states that the device is sterilized using ethylene oxide gas, commonly called E.O. gas.
These are the manufacturer’s published specifications for that particular listing. They should be checked against the packaging and documents for the stock being purchased.
A web page can help buyers identify a product, but it cannot confirm the condition of an individual shipment. Clear labels, matching specifications and complete delivery records remain useful checks when goods arrive.
Infusion Sets and Other Supplies
The company also has a dedicated website listing for a disposable infusion set. Its homepage places IV sets among its main product categories.
DRAP’s registration list separately identifies a Clinic I.V. Infusion Set and a Clinic Blood Transfusion Set. These entries show that the documented range extends beyond syringes.
For purchasing teams, separate product descriptions matter. An order should name the exact set required rather than use a broad phrase such as “IV supplies.” That makes it easier to compare quotations, inspect deliveries and resolve questions with a supplier.
What DRAP Records Can Tell You
DRAP, the Drug Regulatory Authority of Pakistan, publishes records that connect named medical devices with manufacturers and registration numbers. Surgi Plast appears in those records for several CLINIC products.
Registration information is a useful reference, but a complete check also considers later regulatory notices. A historical product entry does not explain whether a particular batch has since become subject to a recall.
The practical approach is to match the product name and registration details, then review relevant safety updates. Each document answers a different question about the item.
The Batch-Specific Safety Alerts in 2026
On 22 May 2026, DRAP published a recall alert naming Clinic Auto Disable Syringe 3 mL/cc, registration number MDMR-000115, in batches 3-01C-26 and 3-01B-26. The notice said samples failed testing of the reuse-prevention feature and were declared substandard.
A further alert dated 8 June 2026 identified batch 3-01B-26 following failure of the auto-disability test. DRAP advised holders of affected stock to stop using it and contact the supplier, distributor or manufacturer for return or replacement.
These notices identify particular products and batches. Their stated scope should guide how they are described and acted upon.
What Buyers Should Check
A useful purchasing record should make the product easy to identify later. Keep the supplier’s invoice, product description and batch information together. That makes stock checks more manageable if a quality question arises.
Before accepting a delivery, compare the ordered specification with the supplied item. Ask the supplier to resolve missing or unclear details rather than filling the gaps with assumptions.
For the affected batches named in its notices, DRAP specifically directs pharmacies and medical stores to stop supply, quarantine remaining stock and return it to the supplier or company. Healthcare facilities should follow the relevant recall instructions.
Conclusion
Surgi Plast has a documented place in Pakistan’s medical disposables sector through its CLINIC syringes and infusion-related products. Understanding the business means looking closely at the devices, their specifications and their regulatory records.
The 2026 batch-specific alerts are also part of that picture. For readers and buyers, the most useful information is precise: which product, which size, which registration and which batch. Those details support a clearer assessment than general praise or a brand name alone.
(FAQs)
What does Surgi Plast manufacture?
Its published range includes syringes and infusion supplies. DRAP records identify several CLINIC-branded devices made by the company, including auto-disable syringes and blood transfusion sets.
Where is Surgi Plast located?
The company lists its address in Gadoon Amazai Industrial Estate, District Swabi, Khyber Pakhtunkhwa, Pakistan.
Which brand is linked with Surgi Plast?
CLINIC is the brand appearing on several Surgi Plast products in DRAP’s published registration list.
Can an auto-disable syringe be reused?
It is designed to become unusable after one use. A suspected failure of that mechanism is a quality concern; it does not make reuse acceptable.
Have any CLINIC syringes been recalled?
Yes. DRAP’s May 2026 alert identified 3 mL/cc Clinic Auto Disable Syringe batches 3-01C-26 and 3-01B-26. Buyers should compare exact batch numbers with the official notice.
