Interacoustics Equinox Evo
Ref 8533212
Interacoustics Equinox Evo is a device classified as Class IIa in the EU and Class II in the US made by Interacoustics A/S, registered in EUDAMED on 14 Oct 2026 (Basic UDI-DI 5711117_8533212_6D) and listed in FDA GUDID since 17 Mar 2025 (UDI-DI 05711117227529), active as of 7 Nov 2026.
Active
CE MDR
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number5711117_8533212_6D 05711117227529 | Date14 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number05711117227529 | Date17 Mar 2025 | StatusListed |
Official records
- EUDAMED public site 5711117_8533212_6D
- AccessGUDID record 05711117227529
Across registries
- EUDAMED Basic UDI-DI 5711117_8533212_6D registered 14 Oct 2026 Active
- FDA GUDID UDI-DI 05711117227529 listed 17 Mar 2025 Listed
Timeline
- Listed FDA GUDID 05711117227529
- Registered EUDAMED 5711117_8533212_6D
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Interacoustics Equinox Evo EUDAMEDInteracoustics GUDID
- Generic name
- Vestibulo-auditory analysis system
- Device name
- Equinox Evo
- Model / reference
- 8533212 EUDAMEDEquinox Evo GUDID
- Primary DI / UDI-DI
- 05711117227529
- Basic UDI-DI
- 5711117_8533212_6D
- Direct marketing DI
- 05711117227529
- FDA product code
- EWO
- EMDN code
- Z121401 Audiometers
- GMDN term
- Vestibulo-auditory analysis system
- Device class
- Class IIa EUDAMEDClass II GUDID
- Regulation number
- 874.1050
- EU registration type
- Standard device
- EU market of registration
- Denmark
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | 8533212 | Equinox Evo |
| Device class | Class IIa | Class II |
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