Oticon 222564
by Oticon A/S
Oticon 222564 is a Class II device made by Oticon A/S, listed in FDA GUDID since 20 May 2020 (UDI-DI 05707131396365), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number05707131396365 | Date20 May 2020 | StatusListed |
Official records
- AccessGUDID record 05707131396365
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Oticon
- Generic name
- Hearing aid wireless-fitting computer-aided set
- Model / reference
- 222564
- Primary DI / UDI-DI
- 05707131396365
- FDA product code
- KLW, OSM
- GMDN term
- Hearing aid wireless-fitting computer-aided set
- Device class
- Class II
- Regulation number
- 874.3400, 874.3305
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
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