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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/2021/000212_95373924478f334ce26c72cd209efd16_5623b76ff9cd55edbb6f45bb46cf7cbe. This device is marketed under the brand name ARNILENE, ARNISTERI LENE. The license holder is Unisur Lifecare 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/2021/000212_95373924478f334ce26c72cd209efd16_5623b76ff9cd55edbb6f45bb46cf7cbe

Brand Name

ARNILENE, ARNISTERI LENE

Device Class

Class C

Approving Authority

Sub Zonal Bangalore

Product Information

Monofilament Polypropylene mesh is used for the repair of hernia, utero-vaginal prolapse and other fascial deficiencies that require the addition of a reinforcing or bridging material to obtain the desired surgical result. It can be used in endoscopic procedures.

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