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Covid -19 neutralizing antibody rapid test for detection of neutralizing antibodies in human serum / plasma / whole blood - India CDSCO Medical Device Registration

Covid -19 neutralizing antibody rapid test for detection of neutralizing antibodies in human serum / plasma / whole blood is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000161_fd3fe740b70b98c27157e259c7dc0fb6_ef674f660a60442f1807a587d613ccfa. This device is marketed under the brand name EzDx. The license holder is ADVY CHEMICAL PVT. LTD., and it is classified as Device Class Class C. The approving authority is Central Drug Standards Control Organization, West Zone.

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CDSCO Registered
Class Class C
Covid -19 neutralizing antibody rapid test for detection of neutralizing antibodies in human serum / plasma / whole blood
UID: MFG/IVD/2020/000161_fd3fe740b70b98c27157e259c7dc0fb6_ef674f660a60442f1807a587d613ccfa

Brand Name

EzDx

Device Class

Class C

Approving Authority

Central Drug Standards Control Organization, West Zone

Product Information

EzDx Covid -19 neutralizing antibody rapid test is used for the detection of neutralizing antibodies in human serum / plasma / Whole blood

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