Yooko HTD2601US
by Hetaida Technology Co., Ltd
Yooko HTD2601US is a Class II device made by Hetaida Technology Co., Ltd, listed in FDA GUDID since 6 Oct 2021 (UDI-DI 06970289035366), 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 | Number06970289035366 | Date6 Oct 2021 | StatusListed |
Official records
- AccessGUDID record 06970289035366
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Yooko
- Generic name
- Nasal aspirator, electric
- Model / reference
- HTD2601US
- Primary DI / UDI-DI
- 06970289035366
- FDA product code
- KDQ
- GMDN term
- Nasal aspirator, electric
- Device class
- Class II
- Regulation number
- 880.6740
- GUDID distribution status
- In Commercial Distribution
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