Retinol Binding Protein Assay Kit (Latex Immunoturbidimetric Method)
by Da Te Bioengineering Technology Co., LTD. 12 variants
Ref DTSH030802Model R1: 21 mL×1; R2: 7 mL×1
Active
CE IVDD
Valid until
Not listed
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/IVDD | NumberB-06975225464248 06975225464248 | Date9 Mar 2023 | StatusActive |
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/IVDD Active
Specification
- Device Name
- Retinol Binding Protein Assay Kit (Latex Immunoturbidimetric Method)
- Model / Reference
- R1: 21 mL×1, R2: 7 mL×1, DTSH030802
- Primary DI / UDI-DI
- 06975225464248
- Basic UDI-DI
- B-06975225464248
- EMDN Code
- W0102010405 Lipoprotein ( a )
- Device Class
- Class IVD General
- EU market of registration
- Netherlands
Manufacturer details
- EUDAMED SRN
- CN-MF-000028832
- Authorised representative
- Lotus NL B.V. NL-AR-000000121
Other devices from Da Te Bioengineering Technology Co., LTD.
See all devices from Da Te Bioengineering Technology Co., LTD. →
Properties
Other properties (7)
- Sterile: No
- Human Tissues: No
- Animal Tissues: No
- Self Testing: No
- Near-Patient Testing: No
- Companion Diagnostics: No
- Surgical Instrument: No