Tempus Pro 01-2068

by Remote Diagnostic Technologies Limited

Tempus Pro 01-2068 is a Class II device made by Remote Diagnostic Technologies Limited, listed in FDA GUDID since 16 Sep 2016 (UDI-DI 05060472440211), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

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	Number05060472440211 UDI-DI	Date16 Sep 2016Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 05060472440211

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Tempus Pro
Generic name: Multiple vital physiological parameter monitoring system, clinical
Model / reference: 01-2068

Primary DI / UDI-DI: 05060472440211
FDA product code: MHX
GMDN term: Multiple vital physiological parameter monitoring system, clinical

Device class: Class II
Regulation number: 870.1025
GUDID distribution status: In Commercial Distribution

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Properties

Prescription use
Lot / batch number
Manufacturing date

Other properties (12, all answered No)