Technicuff UA-1745
by Technicuff Corp. 3 variants
Technicuff UA-1745 is a Class II device made by Technicuff Corp., cleared under FDA 510(k) K942259 on 6 Sep 1994 and listed in FDA GUDID since 14 Sep 2016 (UDI-DI 00819980010103), 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 | Number00819980010103 | Date14 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK942259 | Date6 Sep 1994 | StatusActive |
Official records
- AccessGUDID record 00819980010103
- FDA 510(k) database K942259
Across registries
- FDA 510(k) K942259 decided 6 Sep 1994 Active
- FDA GUDID UDI-DI 00819980010103 listed 14 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K942259
- Listed FDA GUDID 00819980010103
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Technicuff
- Generic name
- Patient monitoring system module, blood pressure, noninvasive
- Model / reference
- UA-1745
- Description
- Adult Blood Pressure Cuff 100 each
- Primary DI / UDI-DI
- 00819980010103
- 510(k) Number
- FDA product code
- DXQ
- GMDN term
- Patient monitoring system module, blood pressure, noninvasive
- Device class
- Class II
- Regulation number
- 870.1120
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Patient monitoring system module, blood pressure, noninvasive.