25-OH-VD Quantitative Test Kit (Time-Resolved FIA)
by Zhejiang Orient Gene Biotech Co., Ltd 3 variants
Ref FIVD-402a-DR10Model FIVD-402a-DR10, FIVD-402a-DR10LH, FIVD-402a-DR10HG, FIVD-402a-DR, FIVD-402a-DRLH, FIVD-402a-DRHG
Active
CE IVDR
Valid until
1 Apr 2030
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/IVDR | Number6188440CE01 | Date1 Sep 2026 | StatusActive |
Certificates
- 6188440TD06 Active
Technical documentation EU IVDR
- Certifier
- DEKRA Certification B.V. 0344
- Issued
- 12 Jan 2026
- Expires
- 1 Jan 2031
- 6188440CE01 Active
Quality management system EU IVDR
- Certifier
- DEKRA Certification B.V. 0344
- Issued
- 1 Sep 2026
- Expires
- 1 Apr 2030
- Reason
- Add device or group
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/IVDR Active
Specification
- Model / Reference
- FIVD-402a-DR10, FIVD-402a-DR10LH, FIVD-402a-DR10HG, FIVD-402a-DR, FIVD-402a-DRLH, FIVD-402a-DRHG
- Primary DI / UDI-DI
- 06950996003902
- Basic UDI-DI
- 69509960FIVD-402a-DRZ9
- Direct Marketing DI
- 06950996003902
- EMDN Code
- W0102060309 25-hydroxyvitamin d
- Device Class
- Class B
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- CN-MF-000017965
- Authorised representative
- CMC Medical Devices & Drugs SL ES-AR-000000293
Other devices from Zhejiang Orient Gene Biotech Co., Ltd.
See all devices from Zhejiang Orient Gene Biotech Co., Ltd. →
Properties
Other properties (8)
- Sterile: No
- Human Tissues: No
- Animal Tissues: No
- Microbial Substances: No
- Self Testing: No
- Companion Diagnostics: No
- Surgical Instrument: No
- New Device: No