CDSCO UID IMP/IVD/2020/000072_fcbf087246e5cfb10e69c9330b8d7ec4_3f0487d7ebe319ddca9fa6b758d9587d

Alpha-fetoprotein

Mindray Medical India Pvt. Ltd.·Device Class Class C·India CDSCO·Brand: CLIA
Registration details
UID
IMP/IVD/2020/000072_fcbf087246e5cfb10e69c9330b8d7ec4_3f0487d7ebe319ddca9fa6b758d9587d
Device class
Class C
Brand name
CLIA
Approving authority
CDSCO
Product information
The CL-series AFP assay is a Chemiluminescent Immunoassay (CLIA) for the quantitative determination of alpha-fetoprotein (CLIA) in human serum or plasma
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 Mindray Medical India Pvt. Ltd.
Products from the same license holder (10 products)
Defibrillator/Monitor
Brand: Mindray
Class C
HbA1c Calibrator
Brand: Mindray
Class B
TRF Calibrator
Brand: Mindray
Class B
Rheumatoid Factor Calibrator
Brand: Mindray
Class B
ADA Control
Brand: Mindray
Class B
HS-CRP
Brand: Mindray
Class B
MALB Calibrator
Brand: Mindray
Class B
TBA Control
Brand: Mindray
Class B
FER Calibrator
Brand: Mindray
Class B
IgE Calibrator
Brand: Mindray
Class B
About this record

Alpha-fetoprotein is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2020/000072_fcbf087246e5cfb10e69c9330b8d7ec4_3f0487d7ebe319ddca9fa6b758d9587d. This device is marketed under the brand name CLIA. The license holder is Mindray Medical India Pvt. Ltd., and it is classified as Device Class Class C. 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.