Pure Global

Blood Collection Tube - Lithium Heparin - India CDSCO Medical Device Registration

Blood Collection Tube - Lithium Heparin is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000154_bd1572e9f4e05f829066e1e4aeb1bc1d_beb6c99478338ce1893a85787b583b9b. This device is marketed under the brand name KRIVIDA - Vacuum Sodium Heparin. The license holder is GAMMA AGRO-MEDICAL PROCESSINGS PVT.LTD, and it is classified as Device Class Class A. The approving authority is Telangana.

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.

Free Database
Powered by Pure Global AI
CDSCO Registered
Class Class A
Blood Collection Tube - Lithium Heparin
UID: MFG/IVD/2022/000154_bd1572e9f4e05f829066e1e4aeb1bc1d_beb6c99478338ce1893a85787b583b9b

Brand Name

KRIVIDA - Vacuum Sodium Heparin

Device Class

Class A

Approving Authority

Telangana

Product Information

A sterile plastic tube, sealed with a stopper, containing a pre-measured amount of vacuum and the anticoagulant lithium heparin. It is intended to be used for the collection, preservation and/or transport, of blood for analysis and/or other investigation (KRIVIDA - Vacuum Sodium Heparin). This is a single-use device

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing