Klipp®
by Kortexx Developpement 12 variants
Ref KL5
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 | Number3770018710KLIPP1A6SSY5 37700187100442 | Date8 Sep 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- Withdrawn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/MDR Active
Specification
- Device Name
- KLIPP® sans indicateur
- Model / Reference
- KL5
- Primary DI / UDI-DI
- 37700187100442
- Basic UDI-DI
- 3770018710KLIPP1A6SSY5
- EMDN Code
- S010499 Sterilisation containers - other
- Device Class
- Class I
- EU market of registration
- France
Manufacturer details
- EUDAMED SRN
- FR-MF-000057587
Other devices from Kortexx Developpement
Properties
Other properties (12)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: 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