Pure Global

Ureter Stent Set - India CDSCO Medical Device Registration

Ureter Stent Set is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2018/000425_ee2cc61b6a2373c21f13e113de43e7fe_b97f143b51a61a974db05461ce823cef. This device is marketed under the brand name Rusch. The license holder is Teleflex Medical Private Limited, and it is classified as Device Class Class C. 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 C
Ureter Stent Set
UID: IMP/MD/2018/000425_ee2cc61b6a2373c21f13e113de43e7fe_b97f143b51a61a974db05461ce823cef

Brand Name

Rusch

Device Class

Class C

Approving Authority

CDSCO

Product Information

Rusch ureter stents are intended for use as routine ureter stents as recommended by a physician or suitably qualified medical personnel. Examples of indications for placement include following ureteric surgery or lithotripsy for ureter stone treatment

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing