- Organization name
- UDI-DI code
- Reference / catalog number
GB-MF-000002127Tempus Pro Configuration Utility Software is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Remote Diagnostic Technologies Ltd.. Placed on the EU market in Norway. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on May 19, 2026
506047244BM731V8Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)05060472440419
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
Primary placement in Norway; available across 19 countries total.
| Country | On market since | Until |
|---|---|---|
| NorwayPrimary placement | Mar 12, 2022 | Dec 31, 9999 |
| Austria | Mar 12, 2022 | Dec 31, 9999 |
| Belgium | Mar 12, 2022 | Dec 31, 9999 |
| Czechia | Mar 12, 2022 | Dec 31, 9999 |
| Germany | Mar 12, 2022 | Dec 31, 9999 |
| Denmark | Mar 12, 2022 | Nov 22, 2023 |
| Spain | Mar 12, 2022 | Dec 31, 9999 |
| France | Mar 12, 2022 | Dec 31, 9999 |
| Croatia | Mar 12, 2022 | Dec 31, 9999 |
| Ireland | Mar 12, 2022 | Dec 31, 9999 |
| Iceland | Mar 12, 2022 | Dec 31, 9999 |
| Italy | Mar 12, 2022 | Dec 31, 9999 |
| Liechtenstein | Mar 12, 2022 | Dec 31, 9999 |
| Luxembourg | Mar 12, 2022 | Dec 31, 9999 |
| Malta | Mar 12, 2022 | Dec 31, 9999 |
| Netherlands | Mar 12, 2022 | Dec 31, 9999 |
| Poland | Mar 12, 2022 | Dec 31, 9999 |
| Sweden | Mar 12, 2022 | Dec 31, 9999 |
| XI | Mar 12, 2022 | Dec 31, 9999 |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
05060472440419Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
506047244BM731V801-2501UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z1203020299MULTI–PARAMETER MONITORS - OTHER506047244BM726VFOn the marketTempus LS Mount506047244BM724VBOn the marketTempus Pro 2-Channel Invasive Pressure Universal Cable506047244BM725VDOn the marketTempus Pro Li-ion Battery506047244BM726VFOn the marketTempus Pro Patient MonitorB-05060472442918On the marketTempus Pro Patient MonitorB-05060472442925On the marketNo certificate specifically references this device's Basic UDI-DI.
Certificate health across this manufacturer's portfolio.
28620139844-01IssuedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
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