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Intrathecal Catheter Pump Segment revision kit - India CDSCO Medical Device Registration

Intrathecal Catheter Pump Segment revision kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2019/000040_c449921f0196aca44e924f67e47995b1_a8091737921a91724aad929676164842. This device is marketed under the brand name Ascenda. The license holder is India Medtronic Private Limited, and it is classified as Device Class Class D. The approving authority is CDSCO.

This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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CDSCO Registered
Class Class D
Intrathecal Catheter Pump Segment revision kit
UID: IMP/MD/2019/000040_c449921f0196aca44e924f67e47995b1_a8091737921a91724aad929676164842

Brand Name

Ascenda

Device Class

Class D

Approving Authority

CDSCO

Product Information

The catheter is part of an infusion system that stores and delivers parenteral drugs to the intrathecal space

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