Piccolo Plus Aero
by Inventis SRL
Part of a family of 6 devices: see the family page
Ref 10330Model Piccolo
Piccolo Plus Aero (10330) is a device classified as Class IIa in the EU and Class II in the US made by Inventis SRL, registered in EUDAMED on 11 Jun 2026 (Basic UDI-DI 805418738AU1PE5) and listed in FDA GUDID since 17 Sep 2016 (UDI-DI 08054187380365), withdrawn as of 23 Oct 2026.
Withdrawn
CE MDR, withdrawn
Ended
Withdrawn
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number805418738AU1PE5 08054187380365 | Date11 Jun 2026 | StatusWithdrawn |
| United States | GUDID listing GUDID | Number08054187380365 | Date17 Sep 2016 | StatusListed |
Official records
- EUDAMED public site 805418738AU1PE5
- AccessGUDID record 08054187380365
Across registries
- EUDAMED Basic UDI-DI 805418738AU1PE5 registered 11 Jun 2026 Withdrawn
- FDA GUDID UDI-DI 08054187380365 listed 17 Sep 2016 Listed
Timeline
- Listed FDA GUDID 08054187380365
- Registered EUDAMED 805418738AU1PE5
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Piccolo Plus Aero EUDAMEDPiccolo GUDID
- Generic name
- Tone audiometer
- Model / Ref / Catalog
- Piccolo, 10330, PICCOLO PLUS AERO
- Primary DI / UDI-DI
- 08054187380365
- Basic UDI-DI
- 805418738AU1PE5
- FDA product code
- EWO
- EMDN code
- Z121401 Audiometers
- GMDN term
- Tone audiometer
- Device class
- Class IIa EUDAMEDClass II GUDID
- Regulation number
- 874.1050
- EU registration type
- Standard device
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | Piccolo 10330 | PICCOLO PLUS AERO |
| Device class | Class IIa | Class II |
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