CDSCO UID MFG/IVD/2023/000145_12ee3a71825a27e1d5ffc0d5423f45e8_08fd9e799976a49c1f0e8a82580c47db

Dengue IgG/IgM Ab Test

Mylab Discovery Solutions Pvt. Ltd.·Device Class Class B·India CDSCO·Brand: SickleCatch™
Registration details
UID
MFG/IVD/2023/000145_12ee3a71825a27e1d5ffc0d5423f45e8_08fd9e799976a49c1f0e8a82580c47db
Device class
Class B
Brand name
SickleCatch™
Approving authority
Kokan Division
Product information
The Dengue IgG/IgM Ab test card is used for rapid visual tests for the qualitative detection of the presence or absence of Antibodies, specific to Dengue IgG/IgM antibody in human whole blood /Serum/Plasma specimens.
Similar products (3)
Other products with the same name or brand
Sickle Cell Rapid Test
Brand: SickleCatch™
Mylab Discovery Solutions Pvt. Ltd.
Class B
S.typhi IgG/IgM Ab Test
Brand: SickleCatch™
Mylab Discovery Solutions Pvt. Ltd.
Class B
Dengue IgG/IgM Ab Test
Brand: hCG
Mylab Discovery Solutions Pvt. Ltd. Lonavla
Class B
Other products from Mylab Discovery Solutions Pvt. Ltd.
Products from the same license holder (10 products)
Sickle Cell Rapid Test
Brand: SickleCatch™
Class B
S.typhi IgG/IgM Ab Test
Brand: SickleCatch™
Class B
Laboratory Instrument/Analyser Application Software, Multipurpose Health Analyzer
Brand: Swayam, Swandook
Class A
Photometric Immunoassay Analyzer
Brand: Swayam, Swandook
Class A
HBsAg Test
Brand: PathoCatchTM
Class D
Nucleic Acid Sample Preparation Instrument
Brand: PCR
Class A
Fluorescent Immunoassay Analyser
Brand: PCR
Class A
Fluorescent Immunoassay Analyser
Brand: PCR
Class A
Nucleic Acid Amplification Analyzer
Brand: PCR
Class A
Nucleic Acid Amplification Analyzer
Brand: PCR
Class A
About this record

Dengue IgG/IgM Ab Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000145_12ee3a71825a27e1d5ffc0d5423f45e8_08fd9e799976a49c1f0e8a82580c47db. This device is marketed under the brand name SickleCatch™. The license holder is Mylab Discovery Solutions Pvt. Ltd., and it is classified as Device Class Class B. 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.