Prophecy® 3 Dg Wedge
Ref PBDEG300
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 | Number0192629IRKL091199A2 00192629131828 | Date3 Nov 2026 | 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- Withdrawn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
- Knee Orthopaedic prosthesis implantation instrument – reusable
- Model / Reference
- PBDEG300
- Primary DI / UDI-DI
- 00192629131828
- Basic UDI-DI
- 0192629IRKL091199A2
- Secondary DI
- M684PBDEG3001
- Direct Marketing DI
- 00192629131828
- EMDN Code
- L091199 Orthopaedic prosthetics instruments, reusable - other
- Device Class
- Class I
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- US-MF-000010240
- Authorised representative
- MicroPort Scientific Coöperatief U.A. NL-AR-000007340
Other devices from MicroPort Orthopedics Inc.
Properties
Other properties (12)
- Sterile: No
- Implantable: 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