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FR-MF-00000755629702DESOCCLUSOL ORANGE is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by ACTEON MANUFACTURING. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Jul 7, 2025
B-03760243000812Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)03760243000812
17 warnings recorded — scroll inside the panel to see all entries.
OTHER
OTHER
OTHER
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 France; available across 15 countries total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Apr 13, 2017 | Dec 31, 2028 |
| Austria | Apr 13, 2017 | Dec 31, 2028 |
| Belgium | Apr 13, 2017 | Dec 31, 2028 |
| Cyprus | Apr 13, 2017 | Dec 31, 2028 |
| Germany | Apr 13, 2017 | Dec 31, 2028 |
| Spain | Apr 13, 2017 | Dec 31, 2028 |
| Croatia | Feb 21, 2025 | Dec 31, 2028 |
| Ireland | Apr 13, 2017 | Dec 31, 2028 |
| Iceland | Apr 13, 2017 | Dec 31, 2028 |
| Liechtenstein | Apr 13, 2017 | Dec 31, 2028 |
| Luxembourg | Apr 13, 2017 | Dec 31, 2028 |
| Netherlands | Apr 13, 2017 | Dec 31, 2028 |
| Poland | Apr 13, 2017 | Dec 31, 2028 |
| Portugal | Apr 13, 2017 | Dec 31, 2028 |
| Sweden | Apr 13, 2017 | Dec 31, 2028 |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
03760243000812Basic 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-03760243000812226022UDI 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.
Q01010299ROOT CANAL FILLING DEVICES - OTHERNo certificate specifically references this device's Basic UDI-DI.
Certificate health across this manufacturer's portfolio.
40031Supplemented39305SupplementedNotified 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 →Notified 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 →