Cardioplegia needle
- UID
- IMP/MD/2020/000403_eaa698c2b6ce5e5ab834972a5662ff51_798ff0ccb674bcb56d0182f71652668a
- Device class
- Class B
- Brand name
- DLP
- 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
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.
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.