Pre Dilatation Catheter - India CDSCO Medical Device Registration
Pre Dilatation Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000321_68a69d17b4cb09d5dbc76459ca91852f_b787ddcd559d2a086a6c02d43541689e. This device is marketed under the brand name FORCE. The license holder is Relisys Medical Device Limited, and it is classified as Device Class Class C. The approving authority is CDSCO, Zonal office, Hyderabad.
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.
Brand Name
FORCE
License Holder
Relisys Medical Device LimitedDevice Class
Approving Authority
CDSCO, Zonal office, Hyderabad
Product Information
Pre-Dilatation Catheter is a minimally invasive procedure to open up blocked coronary arteries, allowing blood to circulate unobstructed to the heart muscle.
Pre Dilatation Catheter
Brand: Serpentile, Serpentile Pro, Serpentile Prime
Relisys Medical Devices Limited
Post Dilatation Catheter
Brand: FORCE
Relisys Medical Device Limited
Pre Dilatation Catheter
Brand: Pearsilk, Silkfil.
Multimedics LLP
Pre Dilatation Catheter
Brand: Invento® NC
Relisys Medical Devices Limited
Pre Dilatation Catheter
Relisys Medical Devices Limited
Post Dilatation Catheter
Brand: FORCE
EVEROLIMUS ELUTING COBALT CHROMIUM CORONARY STENT SYSTEM
Brand: SAVIOUR/TRACK
SIROLIMUS ELUTING CORONARY STENT SYSTEM
Brand: SAVIOUR/TRACK
MANIFOLD
Brand: DELIVER
Guide Extension Catheter
Brand: DELIVER
Guiding Catheter
Brand: DELIVER
Introducer Needle
Brand: DELIVER
Angiographic Diagnostic Catheter
Brand: DELIVER