Technicuff UA-E

by Technicuff Corp. 2 variants

Technicuff UA-E 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 00819980010417), active as of 23 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

FDA submission, from GUDID

Trust

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00819980010417 UDI-DI	Date14 Sep 2016Listed	StatusListed GUDID: in commercial distribution
United States	FDA 510(k)SESE from GUDID Substantially Equivalent · Traditional	NumberK942259	Date6 Sep 1994Decided	StatusActive

Official records

AccessGUDID record UDI-DI 00819980010417
FDA 510(k) database 510(k) number K942259

Across registries

2 registries list this device

FDA 510(k) K942259 decided 6 Sep 1994 Active
FDA GUDID UDI-DI 00819980010417 listed 14 Sep 2016 Listed

Timeline

2 dated events

6 Sep 1994 Cleared FDA 510(k) K942259
14 Sep 2016 Listed FDA GUDID 00819980010417

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name: Technicuff
Generic name: Patient monitoring system module, blood pressure, noninvasive
Model / reference: UA-E

Primary DI / UDI-DI: 00819980010417
510(k) Number: K942259
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.

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Properties

Lot / batch number

Other properties (14, all answered No)