Safety lancet
by Tianjin Huahong Technology Co., Ltd. 177 variants
Ref NoModel XIII, XVII, XXI, XXII, XXIII, XXIV, XXV, XXVIII, XXX, XXXIV, XXXVI
Active
CE MDR
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/MDR | Number69571386SL02WU 06957138605369 | Date8 Jun 2023 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Safety lancet
- Model / Reference
- XIII, XVII, XXI, XXII, XXIII, XXIV, XXV, XXVIII, XXX, XXXIV, XXXVI, No
- Primary DI / UDI-DI
- 06957138605369
- Basic UDI-DI
- 69571386SL02WU
- Unit of Use DI
- 06957138605390
- EMDN Code
- V010401 Lancets with safety systems, single-use
- Device Class
- Class IIa
- EU market of registration
- France
Manufacturer details
- EUDAMED SRN
- CN-MF-000015849
- Authorised representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Other devices from Tianjin Huahong Technology Co., Ltd.
Properties
Other properties (12)
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No