Blood Glucose Monitoring System
by Bioland Technology Ltd. 2 variants
Ref G-425-3
Active
CE IVDD 510(k)
Valid until
Not listed
FDA recalls
None foundTrust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/IVDD EUDAMED | NumberB-06939184631578 | Date31 Mar 2025 | StatusActive |
| United States | FDA 510(k) 510(k) | NumberK202739 | Date12 Aug 2022 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Recalls
No FDA recalls found in the data synced 25 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- United States
- European Union
Specification
- Model / Reference
- G-425-3
- Primary DI / UDI-DI
- 06939184631578, 06939184631431, 06939184631585
- Basic UDI-DI
- B-06939184631578, B-06939184631431, B-06939184631585
- EMDN Code
- W0201060102 Blood glucose meters
- Device Class
- Class IVD Annex II List B
- EU market of registration
- Ireland
Manufacturer details
- EUDAMED SRN
- CN-MF-000010625
- Authorised representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Other devices from Bioland Technology Ltd.
Properties
Other properties (8)
- Sterile: No
- Human Tissues: No
- Animal Tissues: No
- Microbial Substances: No
- Reagent: No
- Near-Patient Testing: No
- Professional Testing: No
- Companion Diagnostics: No