CDSCO UID MFG/IVD/2023/000012_fc160e527aff9b8911f6d120e6d18e6b_8aa5a8f03435d92f4e24ffc831628166
Blood Collection K2 EDTA Tube
ARSH SERUM DIAGNOSIS & BROTHERS COMPANY·Device Class Class A·India CDSCO
Registration details
- UID
- MFG/IVD/2023/000012_fc160e527aff9b8911f6d120e6d18e6b_8aa5a8f03435d92f4e24ffc831628166
- Device class
- Class A
- License holder
- ARSH SERUM DIAGNOSIS & BROTHERS COMPANY
- Approving authority
- Bihar
- Product information
- Primary containment of predetermined volume of blood derived from human or animal body for Clinical hematology test and Blood Centre
Similar products (2)
Other products with the same name or brand
Blood Collection K2 EDTA Tube
AMBICA DIAGNOSTICS
Class A
Blood Collection K2 EDTA Tube
Alliance Med Devices
Class A
Other products from ARSH SERUM DIAGNOSIS & BROTHERS COMPANY
Products from the same license holder (6 products)
Blood Collection ESR Tube
Class A
Blood Collection Fluoride Tube
Class A
Blood Collection 3.8% Sodium Citrate Tube
Class A
Blood Collection K3 EDTA Tube
Class A
Blood Collection 3.2% Sodium Citrate Tube
Class A
Blood Collection Clot Activator Tube
Class A
About this record
Blood Collection K2 EDTA Tube is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000012_fc160e527aff9b8911f6d120e6d18e6b_8aa5a8f03435d92f4e24ffc831628166. The license holder is ARSH SERUM DIAGNOSIS & BROTHERS COMPANY, and it is classified as Device Class Class A. The approving authority is Bihar.
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.