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HEMOGLOBIN REAGENT KIT – MODIFIED ALKALINE HEMATIN METHOD - India CDSCO Medical Device Registration

HEMOGLOBIN REAGENT KIT – MODIFIED ALKALINE HEMATIN METHOD is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000072_f5d50a0023d85da27c18084c10c639cb_9cce21197d9602b51f7e7ca6a47c2338. This device is marketed under the brand name Ultichem. The license holder is Yucca Diagnostics, and it is classified as Device Class Class B. The approving authority is Pune Division.

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CDSCO Registered
Class Class B
HEMOGLOBIN REAGENT KIT – MODIFIED ALKALINE HEMATIN METHOD
UID: MFG/IVD/2022/000072_f5d50a0023d85da27c18084c10c639cb_9cce21197d9602b51f7e7ca6a47c2338

Brand Name

Ultichem

License Holder

Yucca Diagnostics

Device Class

Class B

Approving Authority

Pune Division

Product Information

HEMOGLOBIN Kit is liquid stable reagent kit for the quantitative determination of HEMOGLOBIN in human Blood based on END POINT ALKLINE HEMATIN Method

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