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/2020/000086_349d0790630efab67b3c8cd3d1eeddee_ad58f095e5ae91b1b8c6cb779eb397c2. 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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CDSCO Registered

Class Class C

Pre-Dilatation Catheter

UID: MFG/MD/2020/000086_349d0790630efab67b3c8cd3d1eeddee_ad58f095e5ae91b1b8c6cb779eb397c2

Brand Name

Expanse sheath/ Guide sheath/ Large path

License Holder

Relisys Medical Devices Limited

Device Class

Class C

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