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Antergrade cannula - India CDSCO Medical Device Registration

Antergrade cannula is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2020/000403_8fc6f352f0281f25de03a806cd3182d9_da930b2aada1d60931240af49ef4a0b8. This device is marketed under the brand name DLP. The license holder is India Medtronic Private Limited ,Shed No. 3, Block No. 1, Survey No. 389, 400/2A & 2C, Pudur Main Road, Kuthambakkam - 600124, Poonamallee Taluk, Tiruvallur District ,Tiruvallur Tamil Nadu ,600124 ,India, and it is classified as Device Class Class B. The approving authority is CDSCO.

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CDSCO Registered
Class Class B
Antergrade cannula
UID: IMP/MD/2020/000403_8fc6f352f0281f25de03a806cd3182d9_da930b2aada1d60931240af49ef4a0b8

Brand Name

DLP

Device Class

Class B

Approving Authority

CDSCO

Product Information

This cannula is intended for short term use (DLP) in conjunction with cardiopulmonary bypass surgery for delivering cardioplegia solutions. The cannula may also be used to aspirate air from the aorta at the conclusion of the bypass procedure. The Model 23009 cannula may also be used to monitor pressure in the aorta

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