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Forceps - India CDSCO Medical Device Registration

Forceps is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2023/000445_296245d0fd7a55dcf54d47606aee0d3c_88c78655464914745564f8d7413f7808. This device is marketed under the brand name Guardus® overtube – esophageal. The license holder is STERIS INDIA PVT LTD, and it is classified as Device Class Class B. The approving authority is CDSCO.

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 B
Forceps
UID: IMP/MD/2023/000445_296245d0fd7a55dcf54d47606aee0d3c_88c78655464914745564f8d7413f7808

Brand Name

Guardus® overtube – esophageal

License Holder

STERIS INDIA PVT LTD

Device Class

Class B

Approving Authority

CDSCO

Product Information

The disposable Moray micro forceps is intended to sample tissue from lesions that can occur within and outside the gastrointestinal tract (Guardus® overtube – esophageal)

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