Diagnostic Kit for β-HCG - India CDSCO Medical Device Registration

Diagnostic Kit for β-HCG is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000457_77f6574d423e82c785bd5c2873e767ba_25890a2067247fa5b343d172e4e4f0f3. This device is marketed under the brand name Eoscare. The license holder is M/S CLEAR IMAGING MEDICAL SYSTEM PVT. LTD, and it is classified as Device Class Class B. The approving authority is CDSCO.

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CDSCO Registered

Class Class B

Diagnostic Kit for β-HCG

UID: IMP/IVD/2022/000457_77f6574d423e82c785bd5c2873e767ba_25890a2067247fa5b343d172e4e4f0f3

Brand Name

Eoscare

License Holder

M/S CLEAR IMAGING MEDICAL SYSTEM PVT. LTD

Device Class

Class B

Approving Authority

CDSCO

Product Information

This kit is suitable for in vitro quantitative detection of the concentration of Human Chorionic Gonadotropin β-Subunit (Eoscare) in human serum, plasma and whole blood