Luteinizing Hormone Test Kit - India CDSCO Medical Device Registration

Luteinizing Hormone Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000062_6a904e28741975d74ab5d49d0fb83803_110d46c073ebbdde9c3a4da24634e25b. This device is marketed under the brand name hCG. The license holder is Mylab Discovery Solutions Pvt. Ltd. Lonavla, and it is classified as Device Class Class B. The approving authority is Pune Division.

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CDSCO Registered

Class Class B

Luteinizing Hormone Test Kit

UID: MFG/IVD/2021/000062_6a904e28741975d74ab5d49d0fb83803_110d46c073ebbdde9c3a4da24634e25b

Brand Name

hCG

License Holder

Mylab Discovery Solutions Pvt. Ltd. Lonavla

Device Class

Class B

Approving Authority

Pune Division

Product Information

This product is a lateral flow chromatographic immunoassay for the qualitative detection of LH present in human urine at or above 30 mIU/ml. This test is for in-vitro professional diagnostic use as well as for self-use and intended as an aid to early diagnosis of to detect the rise in LH that happens just before ovulation. This test may help you figure out when you will be ovulating and have the best chances of getting pregnant. It provides only an initial screening test result. More specific alternative diagnosis methods should be performed in order to obtain the confirmation of LH present in specimen

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Luteinizing Hormone Test Kit - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

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