Manual Retraction Kit - India CDSCO Medical Device Registration

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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CDSCO Registered

Class Class B

Manual Retraction Kit

UID: IMP/MD/2019/000064_34870ae467c810535ae2a459fa0e2f42_092b96eb54f7ccb07af04832aaf8df4b

Brand Name

Aortic Punch

License Holder

India Medtronic Private Limited

Device Class

Class B

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