Invision
by Wright Medical Technology, Inc. 15 variants
Ref 60001510
Active
CE MDD
Valid until
No date given
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD | NumberB-00840420171320 00840420171320 | Date5 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- Withdrawn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/MDD Active
Specification
- Device name
- Invision™ Talar Augment 15x10mm Central
- Model / reference
- 60001510
- Primary DI / UDI-DI
- 00840420171320
- Basic UDI-DI
- B-00840420171320
- EMDN code
- P090599 Ankle prostheses - other
- Device class
- Class IIb
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Netherlands
Manufacturer details
- EUDAMED SRN
- US-MF-000025260
- Authorised representative
- Stryker European Operations Limited IE-AR-000000092
Other devices from Wright Medical Technology, Inc.
Properties
Other properties (12)
- Sterilise before use: No
- Reusable: No
- Contains latex: No
- Reprocessed single-use device: No
- Contains CMR substances (carcinogenic, mutagenic or toxic to reproduction): No
- Incorporates a substance derived from human blood or plasma: No
- Contains human tissues or cells: No
- Contains animal tissues or cells: No
- Contains endocrine-disrupting substances: No
- Administering medicine: No
- Measuring function: No
- Incorporates a medicinal substance: No