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Diagnostic Kit for Procalcitonin - India CDSCO Medical Device Registration

Diagnostic Kit for Procalcitonin is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2023/000208_3af1a7038baa53e6c8dabaae3003aa65_6e70e10dabf0cdeacee98e351438352c. This device is marketed under the brand name MyBox SAA. The license holder is Mylab Discovery Solutions Pvt. Ltd., and it is classified as Device Class Class C. The approving authority is CDSCO.

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CDSCO Registered
Class Class C
Diagnostic Kit for Procalcitonin
UID: IMP/IVD/2023/000208_3af1a7038baa53e6c8dabaae3003aa65_6e70e10dabf0cdeacee98e351438352c

Brand Name

MyBox SAA

Device Class

Class C

Approving Authority

CDSCO

Product Information

This kit is suitable for in vitro quantitative detection of the concentration of Procalcitonin (MyBox SAA) in human serum, plasma and whole blood. This product is used for testing in medical and health institutions for the auxiliary diagnosis of systemic bacterial infection and sepsis in clinical practice

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