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CDSCO UID MFG/MD/2022/000321_b36a9a53901cff7a32a0854da5c52f46_13a849c01ee4e8e42ac1e87bfdb243f7

Post Dilatation Catheter

Relisys Medical Device Limited·Device Class Class C·India CDSCO·Brand: FORCE
Registration details
UID
MFG/MD/2022/000321_b36a9a53901cff7a32a0854da5c52f46_13a849c01ee4e8e42ac1e87bfdb243f7
Device class
Class C
Brand name
FORCE
License holder
Relisys Medical Device Limited
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
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Products from the same license holder (9 products)
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MANIFOLD
Brand: DELIVER
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Brand: DELIVER
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Hemostasis Valve Set / Y
Class A
About this record

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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