CDSCO UID IMP/IVD/2021/000085_d8be4f0d244b32df860f380608ceff37_d03e2f2a01d6bf74dd499ac7bdafd9aa

Reaction Module

DIAGNOSTIC CARE AND TRADING PVT LTD·Device Class Class B·India CDSCO·Brand: CLIA
Registration details
UID
IMP/IVD/2021/000085_d8be4f0d244b32df860f380608ceff37_d03e2f2a01d6bf74dd499ac7bdafd9aa
Device class
Class B
Brand name
CLIA
Approving authority
CDSCO
Product information
Reaction Modules required for the implementation of the MAGLUMI assays on the MAGLUMI series Fully-auto chemiluminescence immunoassay analyzer (CLIA).
Similar products (10)
Other products with the same name or brand
Testosterone Assay (Testosterone Assay )
Brand: CLIA
Rapid House
Class B
MYO Assay (MYO Assay )
Brand: CLIA
Rapid House
Class B
Blood Culture Positive Sample Pretreatment Kit
Brand: CLIA
Rapid House
Class B
PRL Assay (PRL Assay )
Brand: CLIA
Rapid House
Class B
Substrate
Brand: CLIA
Rapid House
Class B
FT3 Assay (FT3 Assay )
Brand: CLIA
Rapid House
Class B
Mold Sample Pretreatment Kit
Brand: CLIA
Rapid House
Class B
Z5 LD Lyse
Brand: CLIA
Rapid House
Class B
CK-MB Assay (CK-MB Assay )
Brand: CLIA
Rapid House
Class B
T3 Assay (T3 Assay )
Brand: CLIA
Rapid House
Class B
Other products from DIAGNOSTIC CARE AND TRADING PVT LTD
Products from the same license holder (10 products)
25-OH Vitamin D (Maglumi 25-OH Vitamin D )
Brand: CLIA
Class B
PRL (Maglumi PRL )
Brand: CLIA
Class B
PRG (Maglumi PRG )
Brand: CLIA
Class B
Starter 1+2
Brand: CLIA
Class B
TSH (Maglumi TSH )
Brand: CLIA
Class B
T4 (Maglumi T4 )
Brand: CLIA
Class B
FSH (Maglumi FSH )
Brand: CLIA
Class B
SHBG (Maglumi SHBG )
Brand: CLIA
Class B
FT4 (Maglumi FT4 )
Brand: CLIA
Class B
Light Check
Brand: CLIA
Class B
About this record

Reaction Module is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000085_d8be4f0d244b32df860f380608ceff37_d03e2f2a01d6bf74dd499ac7bdafd9aa. This device is marketed under the brand name CLIA. The license holder is DIAGNOSTIC CARE AND TRADING PVT LTD, 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.