kidney dish
by Finess Healthcare Group Co., Ltd
Ref FN-KD020101G01Model FN-KD02
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number697391169KD02LL 06973911695303 | Date16 Sep 2022 | 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- Withdrawn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/MDR Active
Specification
- Model / Reference
- FN-KD02, FN-KD020101G01
- Primary DI / UDI-DI
- 06973911695303
- Basic UDI-DI
- 697391169KD02LL
- EMDN Code
- V0402 Clinical use trays and bowls
- Device Class
- Class I
- EU market of registration
- Greece
Manufacturer details
- EUDAMED SRN
- CN-MF-000004124
- Authorised representative
- SUNGO Europe B.V. NL-AR-000000247
Other devices from Finess Healthcare Group Co., Ltd
Properties
Other properties (13)
- Sterile: No
- 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