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/2019/000158_b36a9a53901cff7a32a0854da5c52f46_b7b164410e4d2d78b11a4bed6eac0dac. The license holder is Relisys Medical Devices Limited, and it is classified as Device Class Class C. The approving authority is CDSCO, Zonal office, Hyderabad.
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License Holder
Relisys Medical Devices LimitedDevice Class
Approving Authority
CDSCO, Zonal office, Hyderabad
Product Information
1. Balloon dilatation of the stenotic portion of a coronary artery or bypass graft stenosis, for the purpose of improving myocardial perfusion. 2. Balloon dilatation of a coronary artery occlusion, for the purpose of restoring coronary flow in patients with ST-segment elevation myocardial infarction. 3. Balloon dilatation of a stent after implantation
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Post Dilatation Catheter
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