Luteinizing Hormone Test - India CDSCO Medical Device Registration

Luteinizing Hormone Test is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2023/000103_9956ec394fe5490a1acb7f81edf9e9c5_a16c3f93a18ed2ceea9e7695e5d421dd. This device is marketed under the brand name RF-IgM. The license holder is Genovik Biotech Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is Rajasthan.

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CDSCO Registered

Class Class B

Luteinizing Hormone Test

UID: MFG/IVD/2023/000103_9956ec394fe5490a1acb7f81edf9e9c5_a16c3f93a18ed2ceea9e7695e5d421dd

Brand Name

RF-IgM

License Holder

Genovik Biotech Pvt. Ltd.

Device Class

Class B

Approving Authority

Rajasthan

Product Information

Genovik Luteinizing Hormone (RF-IgM) test is intended for the quantitative measurement of Luteinizing Hormone (RF-IgM) in serum or plasma

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Brand: RF-IgM

Genovik Biotech Pvt. Ltd.

Luteinizing Hormone Test - India CDSCO Medical Device Registration

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License Holder

Device Class

Approving Authority

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