Alkaline Phosphatase Assay Kit (NPP Substrate-AMP Buffer Method)
by Maccura Biotechnology Co., Ltd. 7 variants
Ref CH0101203Model CH0101203 CH0105203 CH0800203 CH0801203 CH0802203 CH0803203 CH0804203
Active
CE IVDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/IVDR | Number69506174CH0802036M 06950617448341 | Date15 Oct 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/IVDR Active
Specification
- Model / Reference
- CH0101203 CH0105203 CH0800203 CH0801203 CH0802203 CH0803203 CH0804203, CH0101203
- Primary DI / UDI-DI
- 06950617448341
- Basic UDI-DI
- 69506174CH0802036M
- Direct Marketing DI
- 06950617448341
- EMDN Code
- W01010105 Alkaline phosphatase - total
- Device Class
- Class B
- EU market of registration
- Spain
Manufacturer details
- EUDAMED SRN
- CN-MF-000014618
- Authorised representative
- CMC Medical Devices & Drugs SL ES-AR-000000293
Other devices from Maccura Biotechnology Co., Ltd.
Properties
Other properties (9)
- Sterile: No
- Human Tissues: No
- Animal Tissues: No
- Microbial Substances: No
- Self Testing: No
- Near-Patient Testing: No
- Companion Diagnostics: No
- Surgical Instrument: No
- New Device: No