- Organization name
- UDI-DI code
- Reference / catalog number
BE-MF-0000005714130111178CR MD4.0R GENERAL (SR) SET is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Agfa NV. Placed on the EU market in Belgium. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Aug 13, 2026
B-05414904026793Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)05414904026793
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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 Belgium; available across 32 countries total.
| Country | On market since | Until |
|---|---|---|
| BelgiumPrimary placement | Dec 9, 2009 | Still on market |
| Austria | Dec 9, 2009 | Still on market |
| Bulgaria | Dec 9, 2009 | Still on market |
| Cyprus | Dec 9, 2009 | Still on market |
| Czechia | Dec 9, 2009 | Still on market |
| Germany | Dec 9, 2009 | Still on market |
| Denmark | Dec 9, 2009 | Still on market |
| Estonia | Dec 9, 2009 | Still on market |
| EL | Dec 9, 2009 | Still on market |
| Spain | Dec 9, 2009 | Still on market |
| Finland | Dec 9, 2009 | Still on market |
| France | Dec 9, 2009 | Still on market |
| Croatia | Dec 9, 2009 | Still on market |
| Hungary | Dec 9, 2009 | Still on market |
| Ireland | Dec 9, 2009 | Still on market |
| Iceland | Dec 9, 2009 | Still on market |
| Italy | Dec 9, 2009 | Still on market |
| Liechtenstein | Dec 9, 2009 | Still on market |
| Lithuania | Dec 9, 2009 | Still on market |
| Luxembourg | Dec 9, 2009 | Still on market |
| Latvia | Dec 9, 2009 | Still on market |
| Malta | Dec 9, 2009 | Still on market |
| Netherlands | Dec 9, 2009 | Still on market |
| Norway | Dec 9, 2009 | Still on market |
| Poland | Dec 9, 2009 | Still on market |
| Portugal | Dec 9, 2009 | Still on market |
| Romania | Dec 9, 2009 | Still on market |
| Sweden | Dec 9, 2009 | Still on market |
| Slovenia | Dec 9, 2009 | Still on market |
| Slovakia | Dec 9, 2009 | Still on market |
| Türkiye | Dec 9, 2009 | Still on market |
| XI | Dec 9, 2009 | Still on market |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
05414904026793Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
B-05414904026793E493NUDI 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.
Z11060280DIGITAL COMPUTED RADIOGRAPHY (CR) SYSTEMS - HARDWARE ACCESSORIESNo certificate specifically references this device's Basic UDI-DI.
B-05414904027172On the marketCR MD4.0 GENERAL SET SRB-05414904027165On the marketCR MD4.0R FLFS SETB-05414904026595On the marketCR MD4.0R GENERAL (SR) SETB-05414904026571On the marketCR MD4.0R GENERAL (SR) SETB-05414904026601On the marketCR MD4.0R GENERAL (SR) SETB-05414904026786On the marketCertificate health across this manufacturer's portfolio.
28620125060SupplementedNotified 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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