Blood Collection Tube - India CDSCO Medical Device Registration
Blood Collection Tube is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000151_c223df10ceaedde36ae1eed86c313188_1e41ffd062af09bda1e8d63d1270f182. This device is marketed under the brand name K3 EDTA. The license holder is SPARSH MEDIPLUS, and it is classified as Device Class Class A. The approving authority is Kokan Division.
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.
Brand Name
K3 EDTA
License Holder
SPARSH MEDIPLUSDevice Class
Approving Authority
Kokan Division
Product Information
A device, whether vacuum type or not, specifically intended for the primary containment of predetermined volume of blood derived from human or animal body
Blood Collection Tube
Brand: Fluoride
Virtheal Meditech Private Limited
Blood Collection Tube
Brand: Fluoride
Virtheal Meditech Private Limited
Blood Collection Tube
Brand: Gel with Clot Activator
Agrosurg Irradiators (India) Pvt. Ltd.
Blood Collection Tube
Brand: K3 EDTA
SPARSH MEDIPLUS