Creatinine Reagent test kit
- UID
- MFG/IVD/2022/000015_b7753e67e80b8f2c322fe7768767bbee_5564b2e2b640865fba33b324cf6f7a4d
- Device class
- Class B
- Brand name
- 1:1
- License holder
- DiaSys Diagnostics India Private Limited
- Approving authority
- Kokan Division
- Product information
- Diagnostic reagent for quantitative in vitro determination of Creatinine in human serum or heparin plasma or Urine on automated photometric systems
Creatinine Reagent test kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2022/000015_b7753e67e80b8f2c322fe7768767bbee_5564b2e2b640865fba33b324cf6f7a4d. This device is marketed under the brand name 1:1. 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.