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EUDAMED last updated this device on May 27, 2026
B-04260493310031Multi-Dop X digital with CO2 measuring module is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Compumedics Germany GmbH. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
042604933100317882DE-MF-000005586G10542210015(01)04260493310031
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 Germany; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Jan 1, 2000 | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z12040111BLOOD FLOW METERSPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →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.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →4260493319000VLOn the marketMulti-Dop T4260493318000VDOn the marketMulti-Dop X digitalB-04260493310017On the marketMulti-Dop X digital with Color Doppler imaging moduleB-04260493310024On the marketMulti-Dop X digital with Color Doppler imaging module and CO2 measuring moduleB-04260493310048On the marketMulti-Dop® T4260493318000VDOn the marketNo certificate specifically references this device's Basic UDI-DI.
Certificate health across this manufacturer's portfolio.
G10 054221 0016IssuedNotified 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.
View in glossary →