KUDUwave Pro
KUDUwave Pro is a Class II device made by Emoyodotnetza (Pty) Ltd, listed in FDA GUDID since 2 May 2019 (UDI-DI 06009900487830), registry data as of 22 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 | Number06009900487830 | Date2 May 2019 | StatusListed |
Official records
- AccessGUDID record 06009900487830
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- KUDUwave
- Generic name
- Tone audiometer
- Model / reference
- KUDUwave Pro
- Primary DI / UDI-DI
- 06009900487830
- FDA product code
- EWO
- GMDN term
- Tone audiometer
- Device class
- Class II
- Regulation number
- 874.1050
- GUDID distribution status
- In Commercial Distribution
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