Manufacturing
Our plant in Barabanki, Uttar Pradesh, takes a device from polypropylene granules to a sealed, labelled carton. Every stage runs under our ISO 13485:2016 certified quality management system.
The plant
All 17 products in our catalogue are made at our Barabanki plant.
Components are moulded on site, devices are assembled and packed on our own lines, and sterile products go through our ethylene oxide chamber before release. Keeping these stages together means one team, one set of batch records and no hand-offs between suppliers.
| Address | Khasra No. 22, Village Palta, Deva Road, Barabanki, Uttar Pradesh 225301, India |
|---|---|
| Manufacturing licence | Form MD-5, No. MFG/MD/2026/000291, issued by the State Licensing Authority, Uttar Pradesh |
| Device classes | Class A and Class B, Medical Devices Rules, 2017 (India) |
| Sterilisation | Ethylene oxide (EO), in our own chamber |
| Quality system | ISO 13485:2016 and ISO 9001:2015 certified. View certificates |
| Visits | Plant visits and supplier audits by appointment |
From granule to carton
How a Sterix syringe is made, step by step.
Injection moulding
Barrels, plungers, needle hubs and covers are injection moulded from medical-grade polypropylene on our own machines.
Automated assembly
Automated lines bring the barrel, plunger, gasket and needle together. Operators check the parts and the assembled devices while each batch runs.
Primary packing
Each device is sealed into its own printed ribbon or blister pack. The pack carries the batch number, manufacturing and expiry dates, and our licence number.
Boxing and cartons
Sealed packs are counted into boxes colour-coded by size, then into outer cartons printed with the batch and product details.
EO sterilisation
Products supplied sterile are sterilised with ethylene oxide in our own chamber, then aerated before the batch is released.
Finished goods and dispatch
Released batches move to the finished-goods store and are dispatched against confirmed orders.
Quality checks and traceability
Our quality management system is certified to ISO 13485:2016, the standard for medical device manufacturers. In practice, it works like this.
In-process checks
While a batch is running, we check dimensions, needle gauge and the seal on every pack type.
Final inspection and release
Each batch is inspected and, for sterile products, its sterilisation cycle is confirmed before release. We keep inspection and release records for every batch.
Batch traceability
The batch number printed on every unit pack and carton links it to its production, sterilisation and release records.
Sizes, materials and packing for each device are listed on its product page.
Plan a visit or request documents
Distributors, OEM partners and procurement teams can arrange a plant visit or ask for manufacturing and quality documents.