Pure Global

Fiberscope - India CDSCO Medical Device Registration

Fiberscope is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2023/000244_fcdf259aae855027d02587e28db313db_b7e6d6eececc2e37088c38dd62724200. The license holder is KARL STORZ ENDOSCOPY INDIA PRIVATE LIMITED, 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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class B
Fiberscope
UID: IMP/MD/2023/000244_fcdf259aae855027d02587e28db313db_b7e6d6eececc2e37088c38dd62724200

Device Class

Class B

Approving Authority

CDSCO

Product Information

Flexible intubation endoscopes are intended for endoscopic imaging of the airways, for endotracheal tube placement as well as for bronchoscopy in anesthesia, intensive care and emergency medicine. Flexible intubation endoscopes with working channel enable insertion of non-active instruments in the airways as well as irrigation and suction. Flexible intubation endoscopes are invasive ##PLACEHOLDER_0## and are intended for transient use

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing