AUTOMATED 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.
This page provides comprehensive regulatory information including complete registration details, license holder information, device classification, and related products. Pure Global AI offers free access to 71,807+ India medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.