CEA ELISA(Pathozyme® CEA ELISA) - India CDSCO Medical Device Registration

CEA ELISA(Pathozyme® CEA ELISA) is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2018/000005_a5d6e7f6c40d22d73cf6217461eeb3b6_6095bbc512e638dc575c4276a85bce11. This device is marketed under the brand name Pathozyme® Ovarian Cancer Antigen Ag 125 ELISA. The license holder is Omega DX (Asia) Private Limited, and it is classified as Device Class Class C. The approving authority is CDSCO.

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CDSCO Registered

Class Class C

CEA ELISA(Pathozyme® CEA ELISA)

UID: IMP/IVD/2018/000005_a5d6e7f6c40d22d73cf6217461eeb3b6_6095bbc512e638dc575c4276a85bce11

Brand Name

Pathozyme® Ovarian Cancer Antigen Ag 125 ELISA

License Holder

Omega DX (Asia) Private Limited

Device Class

Class C

Approving Authority

CDSCO

Product Information

Pathozyme® CEA (Pathozyme® Ovarian Cancer Antigen Ag 125 ELISA) ELISA is an in-vitro diagnostic kit used for the quantitative determination of Carcinoembryonic Antigen (Pathozyme® Ovarian Cancer Antigen Ag 125 ELISA)in human serum

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