UREA TEST KIT - India CDSCO Medical Device Registration

UREA TEST KIT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000062_fc39671766533979c0819070eb15ceb3_aaf945455945c156864c3597390ae439. 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

UREA TEST KIT

UID: MFG/IVD/2020/000062_fc39671766533979c0819070eb15ceb3_aaf945455945c156864c3597390ae439

Brand Name

Lateral flow Immunochromatographic Method

License Holder

Mediclone Biotech Private Limited

Device Class

Class B

Approving Authority

Tamil Nadu

Product Information

UREA (Lateral flow Immunochromatographic Method) TEST KIT is used for the quantitative determination of Blood Urea Nitrogen (Lateral flow Immunochromatographic Method) / Urea, based on enzymatic method using Urease and Glutamate dehydrogenase (Lateral flow Immunochromatographic Method) enzymes. This product is used for in vitro diagnosis by professionals

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UREA TEST KIT

Brand: MyBio

Beacon Diagnostics Pvt. Ltd.

UREA TEST KIT - India CDSCO Medical Device Registration

Brand Name

License Holder

Device Class

Approving Authority

Product Information

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UREA TEST KIT

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