AUTOMATED ENZYME IMMUNOASSAY ANALYZER AIA-900 - India CDSCO Medical Device Registration

AUTOMATED ENZYME IMMUNOASSAY ANALYZER AIA-900 is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2022/000332_86afc112248207abb11c323ae0bd68c4_554107c04a9476d60ac3b4903a96d967. This device is marketed under the brand name Tosoh. The license holder is Tosoh India Pvt Ltd, and it is classified as Device Class Class A. The approving authority is CDSCO.

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CDSCO Registered

Class Class A

AUTOMATED ENZYME IMMUNOASSAY ANALYZER AIA-900

UID: IMP/IVD/2022/000332_86afc112248207abb11c323ae0bd68c4_554107c04a9476d60ac3b4903a96d967

Brand Name

Tosoh

License Holder

Tosoh India Pvt Ltd

Device Class

Class A

Approving Authority

CDSCO

Product Information

AIA-900 is an in vitro diagnostic automated anlyzer that measures a variety of substances/anlaytes in serum, plasma, and urine using the AIA-PACK reagent series