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Assayed Human Abnormal Control Plasma for Coagulation Assays - India CDSCO Medical Device Registration

Assayed Human Abnormal Control Plasma for Coagulation Assays is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2021/000021_b33fcc968a5f09deba34e49e3e9f8814_4711fd8ac3763858174c4aa431e5aca4. This device is marketed under the brand name Monospecific Coombs Serum. The license holder is TULIP DIAGNOSTICS PRIVATE LIMITED, and it is classified as Device Class Class C. The approving authority is Sub Zonal Goa.

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CDSCO Registered
Class Class C
Assayed Human Abnormal Control Plasma for Coagulation Assays
UID: MFG/IVD/2021/000021_b33fcc968a5f09deba34e49e3e9f8814_4711fd8ac3763858174c4aa431e5aca4

Brand Name

Monospecific Coombs Serum

Device Class

Class C

Approving Authority

Sub Zonal Goa

Product Information

Abnormal control plasma for calibration and quality control for use with PT, APTT, TT and Fibrinogen assays

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