Basen Bc-022
by Dongguan Yiyingmei Technology Co., Ltd.
Basen Bc-022 is a Class II device made by Dongguan Yiyingmei Technology Co., Ltd., cleared under FDA 510(k) K242028 on 19 Nov 2024 and listed in FDA GUDID since 31 Mar 2025 (UDI-DI 06978331170270), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number06978331170270 | Date31 Mar 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK242028 | Date19 Nov 2024 | StatusActive |
Official records
- AccessGUDID record 06978331170270
- FDA 510(k) database K242028
Across registries
- FDA 510(k) K242028 decided 19 Nov 2024 Active
- FDA GUDID UDI-DI 06978331170270 listed 31 Mar 2025 Listed
Timeline
- Cleared FDA 510(k) K242028
- Listed FDA GUDID 06978331170270
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Basen
- Generic name
- Nasal aspirator, electric
- Model / reference
- BC-022
- Primary DI / UDI-DI
- 06978331170270
- 510(k) Number
- FDA product code
- BTA
- GMDN term
- Nasal aspirator, electric
- Device class
- Class II
- Regulation number
- 878.4780
- GUDID distribution status
- In Commercial Distribution
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