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CDSCO UID IMP/MD/2019/000064_34870ae467c810535ae2a459fa0e2f42_092b96eb54f7ccb07af04832aaf8df4b

Manual Retraction Kit

India Medtronic Private Limited·Device Class Class B·India CDSCO·Brand: Aortic Punch
Registration details
UID
IMP/MD/2019/000064_34870ae467c810535ae2a459fa0e2f42_092b96eb54f7ccb07af04832aaf8df4b
Device class
Class B
Brand name
Aortic Punch
License holder
India Medtronic Private Limited
Approving authority
CDSCO
Product information
The intended purpose of the MRK is to aid manual retraction of the balloon catheter in unlikely situations when standard catheter retraction methods cannot be used
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About this record

Manual Retraction Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000064_34870ae467c810535ae2a459fa0e2f42_092b96eb54f7ccb07af04832aaf8df4b. This device is marketed under the brand name Aortic Punch. The license holder is India Medtronic Private Limited, and it is classified as Device Class Class B. The approving authority is CDSCO.

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