CDSCO UID MFG/IVD/2020/000063_df709c23a914180a03651f080a6a35f0_498782ca38fba3b599782fcf7a0ae3d6
Creatinine Reagent Kit
Kee Diagnostics Pvt. Ltd.·Device Class Class B·India CDSCO
Registration details
- UID
- MFG/IVD/2020/000063_df709c23a914180a03651f080a6a35f0_498782ca38fba3b599782fcf7a0ae3d6
- Device class
- Class B
- License holder
- Kee Diagnostics Pvt. Ltd.
- Approving authority
- South West Delhi Division
- Product information
- For the use of Quantitative determination of Creatinine in serum/plasma or urine
Other products from Kee Diagnostics Pvt. Ltd.
Products from the same license holder (10 products)
Urea Berthelot
Class B
ALT
Class B
Uric Acid Reagent Kit
Class B
Creatine Kinase
Class B
Free T3 ELISA Kit
Class B
Cholinesterase Reagent Kit
Class B
Rheumatoid factors Test
Class B
Haemoglobin - CMG
Class B
Albumin
Class B
Free T4 ELISA Kit
Class B
About this record
Creatinine Reagent Kit is a medical device registered with India's Central Drugs Standard Control Organization (CDSCO) under UID MFG/IVD/2020/000063_df709c23a914180a03651f080a6a35f0_498782ca38fba3b599782fcf7a0ae3d6. The license holder is Kee Diagnostics Pvt. Ltd., and it is classified as Device Class Class B. The approving authority is South West Delhi 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.