REAGENT PACK FOR 931AT/FT
- UID
- IMP/IVD/2021/000330_16f32527792a768510c628b33510126d_22668c9db182530d5a812e7c98ad88db
- Device class
- Class B
- Brand name
- CARETIUM
- License holder
- LAB X
- Approving authority
- CDSCO
- Product information
- For in vitro diagnostic use only , Use for only with XI-931 series electrolyte analyzers
REAGENT PACK FOR 931AT/FT is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID IMP/IVD/2021/000330_16f32527792a768510c628b33510126d_22668c9db182530d5a812e7c98ad88db. This device is marketed under the brand name CARETIUM. The license holder is LAB X, and it is classified as Device Class Class B. 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.