CDSCO UID IMP/IVD/2022/000332_86afc112248207abb11c323ae0bd68c4_554107c04a9476d60ac3b4903a96d967AUTOMATED ENZYME IMMUNOASSAY ANALYZER AIA-900
- UID
- IMP/IVD/2022/000332_86afc112248207abb11c323ae0bd68c4_554107c04a9476d60ac3b4903a96d967
- Device class
- Class A
- Brand name
- Tosoh
- License holder
- Tosoh India Pvt Ltd
- 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
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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