Pure Global

Monofilament Polytetrafluoroethylene suture, non absorbable surgical suture. - India CDSCO Medical Device Registration

Monofilament Polytetrafluoroethylene suture, non absorbable surgical suture. is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2021/000218_0aa1f975616a5991ba2b9ae2f05848e2_ec16b9022bd115a2ccc42b80673778b7. 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class C
Monofilament Polytetrafluoroethylene suture, non absorbable surgical suture.
UID: MFG/MD/2021/000218_0aa1f975616a5991ba2b9ae2f05848e2_ec16b9022bd115a2ccc42b80673778b7

Brand Name

CORESTEEL

Device Class

Class C

Approving Authority

Sub Zonal Bangalore

Product Information

It is indicated for use in all types of soft tissue approximation and/ or ligation, including dental and general surgeries. The device is not indicated for the use in cardiovascular, ophthalmic surgery and peripheral neural tissue

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing