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Cardioplegia needle - India CDSCO Medical Device Registration

Cardioplegia needle is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/MD/2020/000403_eaa698c2b6ce5e5ab834972a5662ff51_798ff0ccb674bcb56d0182f71652668a. 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
Cardioplegia needle
UID: IMP/MD/2020/000403_eaa698c2b6ce5e5ab834972a5662ff51_798ff0ccb674bcb56d0182f71652668a

Brand Name

DLP

Device Class

Class B

Approving Authority

CDSCO

Product Information

These are intended for use in conjunction with cardiopulmonary bypass surgery for up to six hours or less for delivering cardioplegia solution. Only Model 10313 may be used to aspirate air from the aorta during the de-airing procedure

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