LYSE - India CDSCO Medical Device Registration

LYSE is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/MD/2020/000017_6336504f29cd0ee4960364059a3929a7_04b1ea1c81b7172aea6202cd7085d7f6. This device is marketed under the brand name SEROCON CYSTATIN C CONTROL SET. The license holder is Beacon Diagnostics Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Gujarat.

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.

Free Database

CDSCO Registered

Class Class B

LYSE

UID: MFG/MD/2020/000017_6336504f29cd0ee4960364059a3929a7_04b1ea1c81b7172aea6202cd7085d7f6

Brand Name

SEROCON CYSTATIN C CONTROL SET

License Holder

Beacon Diagnostics Pvt. Ltd.

Device Class

Class B

Approving Authority

Gujarat

Product Information

Lyse for B COUNT 3 3-part differential blood cell counters

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

LYSE

Brand: CRP

DELTA LAB

LYSE - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

DJ Fang

LYSE

HBA1C CONTROL SET

PROTEIN CONTROL

PROTEIN CONTROL

UREA UV TEST KIT

FEBRILE S. TYPHI O ANTIGEN(SEROCON FEBRILE S. TYPHI O ANTIGEN )

CHOLINESTERASE

RETIC TUBE

AMYLASE TEST KIT(LIQUIZYME α AMYLASE )

IgG(SEROCON IMMUNOGLOBULIN G TURBILATEX)

HBA1C CONTROL SET

PROTEIN CONTROL

PROTEIN CONTROL

UREA UV TEST KIT

COAGULATION ANALYZER

COAGULATION ANALYZER

FEBRILE S. TYPHI O ANTIGEN(SEROCON FEBRILE S. TYPHI O ANTIGEN )

CHOLINESTERASE

RETIC TUBE

AMYLASE TEST KIT(LIQUIZYME α AMYLASE )