Ozeri BP3T
Ozeri BP3T is a Class II device made by Commonpath LLC, listed in FDA GUDID since 27 Oct 2019 (UDI-DI 00815817013255), 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 | Number00815817013255 | Date27 Oct 2019 | StatusListed |
Official records
- AccessGUDID record 00815817013255
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Ozeri
- Generic name
- Automatic-inflation electronic sphygmomanometer, portable, finger
- Model / reference
- BP3T
- Primary DI / UDI-DI
- 00815817013255
- FDA product code
- DXN
- GMDN term
- Automatic-inflation electronic sphygmomanometer, portable, finger
- Device class
- Class II
- Regulation number
- 870.1130
- GUDID distribution status
- In Commercial Distribution
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