KLS Martin
by KLS Martin SE & Co. KG 890 variants
Ref 25-323-03-71
Active
CE MDR
Valid until
24 Apr 2030
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number40576054485Y 04067118023099 | Date13 Oct 2026 | StatusActive |
Certificates
- 20487GB450260901 Active
Technical documentation EU MDR
- Certifier
- DNV MEDCERT GmbH 0482
- Issued
- 1 Sep 2026
- Expires
- 24 Apr 2030
- Reason
- Add device or group
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Orbita plates Ti/PE
- Model / Reference
- 25-323-03-71
- Primary DI / UDI-DI
- 04067118023099
- Basic UDI-DI
- 40576054485Y
- EMDN Code
- P900403 Non-resorbable filling and reconstruction devices
- Device Class
- Class IIb
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000005551
From the manufacturer
Manufacturer's product page: Art.-Nr. 80-042-00-04 maXium® m-Version mit Buchsenmodul für KLS Martin-Zubehör
Other devices from KLS Martin SE & Co. KG
Properties
Other properties (12)
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Sutures: 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