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CDSCO UID MFG/MD/2020/000086_b36a9a53901cff7a32a0854da5c52f46_7374e979e49bf7a334f8bcf6a4dba9a1

Post Dilatation Catheter

Relisys Medical Devices Limited·Device Class Class C·India CDSCO·Brand: Expanse sheath/ Guide sheath/ Large path
Registration details
UID
MFG/MD/2020/000086_b36a9a53901cff7a32a0854da5c52f46_7374e979e49bf7a334f8bcf6a4dba9a1
Device class
Class C
Brand name
Expanse sheath/ Guide sheath/ Large path
License holder
Relisys Medical Devices 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 artery occlusion, 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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About this record

Post Dilatation Catheter is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2020/000086_b36a9a53901cff7a32a0854da5c52f46_7374e979e49bf7a334f8bcf6a4dba9a1. This device is marketed under the brand name Expanse sheath/ Guide sheath/ Large path. 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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