Progesterone/Estradiol (E2) Combined Assay Kit (Fluorescence Immunochromatographic Assay)
by Wuhan Life Origin Biotech Joint Stock Co., Ltd. 4 variants
Ref SF680252Model 25 tests/kit
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-06978502843569 06978502843569 | Date12 Oct 2026 | 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- Withdrawn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
- Austria
- Belgium
- Bulgaria
- Croatia
- Cyprus
- Czechia
- Denmark
- Estonia
- Finland
- France
- Germany
- Greece
- Hungary
- Iceland
- Ireland
- Italy
- Latvia
- Liechtenstein
- Lithuania
- Luxembourg
- Malta
- Netherlands
- Northern Ireland
- Norway
- Poland
- Portugal
- Romania
- Slovakia
- Slovenia
- Spain
- Sweden
- Türkiye
Specification
- Model / Reference
- 25 tests/kit, SF680252
- Primary DI / UDI-DI
- 06978502843569
- Basic UDI-DI
- B-06978502843569
- EMDN Code
- W0102160399 Fertility/pregnancy rt & poc - other
- Device Class
- Class IVD General
- EU market of registration
- Austria
Manufacturer details
- EUDAMED SRN
- CN-MF-000027340
- Authorised representative
- RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202
Other devices from Wuhan Life Origin Biotech Joint Stock Co., Ltd.
See all devices from Wuhan Life Origin Biotech Joint Stock Co., Ltd. →
Properties
Other properties (8)
- Sterile: No
- Human Tissues: No
- Animal Tissues: No
- Microbial Substances: No
- Self Testing: No
- Near-Patient Testing: No
- Companion Diagnostics: No
- Surgical Instrument: No