- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Nov 24, 2021
++EDET0185Rszilikon alapú fül lenyomat anyag 2x800g is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by DETAX GmbH & Co. KG. Placed on the EU market in Hungary. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
+EDET02319102319DE-MF-000005995+EDET023191
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA / IFA support is coming.
1 warning recorded — scroll inside the panel to see all entries.
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 Hungary; available across 8 countries total.
| Country | On market since | Until |
|---|---|---|
| HungaryPrimary placement | — | Still on market |
| Cyprus | — | Still on market |
| Estonia | — | Still on market |
| Ireland | — | Still on market |
| Iceland | — | Still on market |
| Luxembourg | — | Still on market |
| Malta | — | Still on market |
| XI | — | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
Q030499OTOLOGY DEVICES - OTHERPrimary 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 →No certificate specifically references this device's Basic UDI-DI.
No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.++EDET0275SOn the marketSolflex prov A3 500 g++EDET0275SOn the marketSteramould Plus 2 x 330 g++EDET0185ROn the marketT-Mischer pink BulkBox 6.000 pcs.++EDET0305FOn the markettempofit semi A3 Standardpackung++EDET0976FOn the marketTwinprint Ortho/Splint UV 1000 g++EDET0465WOn the market