Cortisol ELISA - India CDSCO Medical Device Registration

Cortisol ELISA is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000467_5918356b286e01c15750755af1207710_f698388978befce2c71c7eae03b43467. This device is marketed under the brand name Cortisol ELISA. The license holder is CPC DIAGNOSTICS 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

Cortisol ELISA

UID: IMP/IVD/2022/000467_5918356b286e01c15750755af1207710_f698388978befce2c71c7eae03b43467

Brand Name

Cortisol ELISA

License Holder

CPC DIAGNOSTICS PVT.LTD

Device Class

Class B

Approving Authority

CDSCO

Product Information

Competitive immunoenzymatic colorimetric method for quantitative determination of Cortisol concentration in human serum or plasma. Cortisol ELISA kit is intended for laboratory use only,17OH PROGESTERONE ELISA(Cortisol ELISA)-17OH Progesterone ELISA is a manual in vitro diagnostic device intended for the quantitative determination of 17OH Progesterone in human serum or plasma. Results are to be used in conjunction with other clinical and laboratory data as an aid in the diagnosis and monitoring of various disorders of the adrenal glands