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Enter your Product Code and Batch Number — both printed on your product packaging — to view the IFU applicable to your specific batch, in your language.
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About Futura Medtech
Trusted manufacturer of regulated medical devices.
Decades of regulatory experience
Manufacturing medical devices to ISO 13485 and EU MDR standards. Every device we ship carries a fully traceable batch record from raw material to delivery.
Reach across 85+ countries
Our sutures, meshes, and ligation clips are used in operating theatres on every continent. Local regulatory registrations in over 85 markets.
Quality-first culture
ISO 13485 certified QMS, biocompatibility testing to ISO 10993, and EtO sterilisation validated to ISO 11135 — checked on every batch we release.
Built for clinicians
Designed in partnership with surgeons and OR teams. Sterile, single-use, ready-to-open packaging with clear product identification on every label.
Multi-market certified
CE-marked under EU MDR 2017/745 (Notified Body 2460), US-cleared by FDA 510(k), and licensed by CDSCO India under MD-9. Audited annually.
Always within reach
A regulatory team you can talk to. Free paper IFU copies within 7 days under EU 2021/2226 Art. 6 — just submit a request.
Can't find your product code?
Look for the product code and batch number on the box, pouch, or label of your device. Our regulatory team is happy to help if you're stuck.