HEMOGLOBIN TEST REAGENT KIT - SICKLE CELL TEST - India CDSCO Medical Device Registration

HEMOGLOBIN TEST REAGENT KIT - SICKLE CELL TEST is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000062_a4ebfb52b822b21a5d78fa5f1e1c4a7f_2fdd58a6896f02d14b7915784adad14b. This device is marketed under the brand name Lateral flow Immunochromatographic Method. The license holder is Mediclone Biotech Private Limited, and it is classified as Device Class Class B. The approving authority is Tamil Nadu.

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CDSCO Registered

Class Class B

HEMOGLOBIN TEST REAGENT KIT - SICKLE CELL TEST

UID: MFG/IVD/2020/000062_a4ebfb52b822b21a5d78fa5f1e1c4a7f_2fdd58a6896f02d14b7915784adad14b

Brand Name

Lateral flow Immunochromatographic Method

License Holder

Mediclone Biotech Private Limited

Device Class

Class B

Approving Authority

Tamil Nadu

Product Information

The sickle cell test kit is intended to be used as a qualitative detection kit for Hemoglobin S (Lateral flow Immunochromatographic Method) present in sickle red blood cells of anemic blood thorough ?solubility test? method. This product is used for in vitro diagnosis by professionals

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UREA TEST KIT

Brand: Lateral flow Immunochromatographic Method

Mediclone Biotech Private Limited

HEMOGLOBIN TEST REAGENT KIT - SICKLE CELL TEST - India CDSCO Medical Device Registration

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License Holder

Device Class

Approving Authority

Product Information

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