Mobi 700027
Mobi 700027 is a Class II device made by Mobi Technologies, Inc., listed in FDA GUDID since 31 Jul 2022 (UDI-DI 00891040000279), 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 | Number00891040000279 | Date31 Jul 2022 | StatusListed |
Official records
- AccessGUDID record 00891040000279
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Mobi
- Generic name
- Automatic-inflation electronic sphygmomanometer, portable, arm/wrist
- Model / reference
- 700027
- Primary DI / UDI-DI
- 00891040000279
- FDA product code
- DXN
- GMDN term
- Automatic-inflation electronic sphygmomanometer, portable, arm/wrist
- Device class
- Class II
- Regulation number
- 870.1130
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
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