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AUTOMATED ENZYME IMMUNOASSAY SYSTEM AIA-360 - India CDSCO Medical Device Registration

AUTOMATED ENZYME IMMUNOASSAY SYSTEM AIA-360 is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000110_c458d5a82bda0040a863a5c8a98e60d6_4c4599863e74ddca07ec0119b36a441c. This device is marketed under the brand name Tosoh India. The license holder is Tosoh India Pvt. Ltd., and it is classified as Device Class Class A. The approving authority is Kokan Division.

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CDSCO Registered
Class Class A
AUTOMATED ENZYME IMMUNOASSAY SYSTEM AIA-360
UID: MFG/IVD/2022/000110_c458d5a82bda0040a863a5c8a98e60d6_4c4599863e74ddca07ec0119b36a441c

Brand Name

Tosoh India

License Holder

Tosoh India Pvt. Ltd.

Device Class

Class A

Approving Authority

Kokan Division

Product Information

AIA-360 is an in vitro diagnostic automated analyzer that measures a variety of substances/analytes in serum, plasma, and urine using the AIA-PACK reagent series.

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