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Diagnostics test reagent / kits prolactin Test Kit - India CDSCO Medical Device Registration

Diagnostics test reagent / kits prolactin Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000163_ff9f5f3efca3bf025acf2e6ea95292f6_155779d6d50c137412f89f9f591ecd14. This device is marketed under the brand name hCG. The license holder is M/s Allied Biotechnology India Pvt Ltd, and it is classified as Device Class Class B. The approving authority is Kokan Division.

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Class Class B
Diagnostics test reagent / kits prolactin Test Kit
UID: MFG/IVD/2020/000163_ff9f5f3efca3bf025acf2e6ea95292f6_155779d6d50c137412f89f9f591ecd14

Brand Name

hCG

Device Class

Class B

Approving Authority

Kokan Division

Product Information

PRL Test Kit (hCG) is intended for in-vitro quantitative measurement of PRL (hCG) in serum. Clinically, it is mainly used to evaluate the endocrine function of pituitary gland

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