- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 9, 2026
++B844REUSABLECURETTESG3Apical Root Elevator Fig.304 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Trimed (Pvt) Ltd. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
PK-MF-000011692+B84461198340E
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA / IFA support is coming.
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 9 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | — | Still on market |
| Estonia | — | Still on market |
| Spain | — | Still on market |
| France | — | Still on market |
| Italy | — | Still on market |
| Malta | — | Still on market |
| Poland | — | Still on market |
| Portugal | — | Still on market |
| Türkiye | — | 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.
+B84461198340EBasic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
++B844REUSABLECURETTESG361-198-34UDI 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.
L1505ODONTOSTOMATOLOGY LEVERS, REUSABLEPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →++B844REUSABLERETRACTOR2WOn the marketAllison Lung Spatula 32.0cm++B844REUSABLERETRACTOR2WOn the marketApical Root Elevator Fig.301++B844REUSABLECURETTESG3On the marketApical-Flohr Root Elevator Fig.302++B844REUSABLECURETTESG3On the marketArruga Caspular Forcep 10.0cm++B844REUSABLEFORCEPSV3On the marketArruga Caspular Forcep 10.0cm++B844REUSABLEFORCEPSV3On the marketNo certificate specifically references this device's Basic UDI-DI.
Certificate health across this manufacturer's portfolio.
PK25/00000098IssuedNotified 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 →