CDSCO UID MFG/IVD/2022/000015_e6e2fa71f830e8a8d15aea072fb91e68_1c29d412efd1bdc932d2393707d95082
CK NAC Reagent Test Kit
DiaSys Diagnostics India Private Limited·Device Class Class B·India CDSCO
Registration details
- UID
- MFG/IVD/2022/000015_e6e2fa71f830e8a8d15aea072fb91e68_1c29d412efd1bdc932d2393707d95082
- Device class
- Class B
- License holder
- DiaSys Diagnostics India Private Limited
- Approving authority
- Kokan Division
- Product information
- Diagnostic reagent for in vitro quantitative determination of CK NAC in human serum or plasma on photometric analyzers
Similar products (1)
Other products with the same name or brand
CK NAC Reagent Test Kit
M/s JITM C Genes Private Limited
Class B
Other products from DiaSys Diagnostics India Private Limited
Products from the same license holder (10 products)
Alkaline Phosphatase Mono Reagent Test Kit
Class B
Calcium Test Kit
Class B
Calcium standard kit
Class B
Creatinine Standard Test Kit
Class B
Lipase Test Kit
Class B
Triglycerides Test Kit
Class B
Albumin test kit
Class B
Bilirubin Jendrassik Reagent Test Kit
Class B
Urea Standard Kit
Class B
Glucose liquid Test Kit
Class B
About this record
CK NAC Reagent Test Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000015_e6e2fa71f830e8a8d15aea072fb91e68_1c29d412efd1bdc932d2393707d95082. The license holder is DiaSys Diagnostics India Private Limited, and it is classified as Device Class Class B. The approving authority is Kokan Division.
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.