Post Dilatation Catheter - India CDSCO Medical Device Registration

Post Dilatation Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2022/000321_b36a9a53901cff7a32a0854da5c52f46_13a849c01ee4e8e42ac1e87bfdb243f7. 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.

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CDSCO Registered

Class Class C

Post Dilatation Catheter

UID: MFG/MD/2022/000321_b36a9a53901cff7a32a0854da5c52f46_13a849c01ee4e8e42ac1e87bfdb243f7

Brand Name

FORCE

License Holder

Relisys Medical Device Limited

Device Class

Class C

Approving Authority

CDSCO, Zonal office, Hyderabad

Product Information

1.1. Balloon dilatation of the stenotic portion of a coronary artery or bypass graft stenosis, for the purpose of improving myocardial perfusion. 1.2. Balloon dilatation of a coronary arteryocclusion, for the purpose of restoring coronary flow in patients with ST-segment elevation myocardial infarction. 1.3. Balloon dilatation of a stent after implantation