Beurer BR10
Beurer BR10 (603.26) is a Class II device made by Beurer North America, L.P., listed in FDA GUDID since 29 Mar 2023 (UDI-DI 00810110200050), 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 | Number00810110200050 | Date29 Mar 2023 | StatusListed |
Official records
- AccessGUDID record 00810110200050
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Beurer
- Generic name
- Insect bite/sting hyperthermia device
- Model / Ref / Catalog
- BR10, 603.26
- Primary DI / UDI-DI
- 00810110200050
- FDA product code
- IRT
- GMDN term
- Insect bite/sting hyperthermia device
- Device class
- Class II
- Regulation number
- 890.5740
- GUDID distribution status
- In Commercial Distribution
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