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Monofilament polypropylene mesh - India CDSCO Medical Device Registration

Monofilament polypropylene mesh is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2021/000218_9bb63fe3cdfcc5606754732f81b5bb95_3785f88a71b20993590f84b0bf38362c. This device is marketed under the brand name CORESTEEL. The license holder is FUTURA SURGICARE PVT LTD, and it is classified as Device Class Class C. The approving authority is Sub Zonal Bangalore.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class C
Monofilament polypropylene mesh
UID: MFG/MD/2021/000218_9bb63fe3cdfcc5606754732f81b5bb95_3785f88a71b20993590f84b0bf38362c

Brand Name

CORESTEEL

Device Class

Class C

Approving Authority

Sub Zonal Bangalore

Product Information

Mesh is used in hernia repair and weak tissue support

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