CDSCO UID IMP/MD/2019/000368_6cd021cdc05a98e1d17375de78458475_6730d2b13fa6e4153f6780aea30c0553

Target Eluting Coronary Stent System

Reinvent Medical Pvt. Ltd·Device Class Class D·India CDSCO·Brand: FirehawkTM Rapamycin Target Eluting Coronary Stent System
Registration details
UID
IMP/MD/2019/000368_6cd021cdc05a98e1d17375de78458475_6730d2b13fa6e4153f6780aea30c0553
Device class
Class D
Brand name
FirehawkTM Rapamycin Target Eluting Coronary Stent System
Approving authority
CDSCO
Product information
The FirehawkTM Rapamycin Target Eluting Coronary Stent System is indicated for improving coronary luminal diameter in patients with symptomatic heart disease due to de novo native coronary artery lesions length ≤ 60 mm with reference vessel diameters of ≥ 2.25 to ≤ 4.0 mm
Similar products (3)
Other products with the same name or brand
Rapamycin Target Eluting Coronary Stent System
Brand: FirehawkTM Rapamycin Target Eluting Coronary Stent System
Reinvent Medical Pvt. Ltd
Class D
PTCA Balloon Catheter
Brand: FirehawkTM Rapamycin Target Eluting Coronary Stent System
Reinvent Medical Pvt. Ltd
Class D
Target Eluting Coronary Stent System
Brand: FirehawkTM Rapamycin Target Eluting Coronary Stent System
MicroPort Scientific India Pvt. Ltd., ,Shop No. 9, Kamla Palace, Civil Line, Barfkhana ,Gurgaon Haryana ,122001 ,India
Class D
Other products from Reinvent Medical Pvt. Ltd
Products from the same license holder (2 products)
Rapamycin Target Eluting Coronary Stent System
Brand: FirehawkTM Rapamycin Target Eluting Coronary Stent System
Class D
PTCA Balloon Catheter
Brand: FirehawkTM Rapamycin Target Eluting Coronary Stent System
Class D
About this record

Target Eluting Coronary Stent System is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000368_6cd021cdc05a98e1d17375de78458475_6730d2b13fa6e4153f6780aea30c0553. This device is marketed under the brand name FirehawkTM Rapamycin Target Eluting Coronary Stent System. The license holder is Reinvent Medical Pvt. Ltd, and it is classified as Device Class Class D. The approving authority is CDSCO.

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