- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 18, 2026
++B844REUSABLEFORCEPSV3Mathieu Instruments 20.0cm 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+B844197202003
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.
+B844197202003Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
++B844REUSABLEFORCEPSV319-720-20UDI 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.
L03130402FORCEPS FOR EXTERNAL BODIES, 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 →No certificate specifically references this device's Basic UDI-DI.
++B844REUSABLERETRACTOR2WOn the marketMartin-Langenbeck Elevator 20.0cm 10.0mm++B844REUSABLERETRACTOR2WOn the marketMartin-Langenbeck Elevator 20.0cm 8.0mm++B844REUSABLERETRACTOR2WOn the marketMathieu Instruments 28.0cm++B844REUSABLEFORCEPSV3On the marketMaumenee (Colibri) Fixation Forcep 1:2 Teeth 0.12mm 10.0cm++B844REUSABLEFORCEPSV3On the marketMayo – Blake Gall Stone Forcep Cur 20.0cm++B844REUSABLEFORCEPSV3On the marketCertificate 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 →