- Organization name
- UDI-DI code
- Reference / catalog number
DE-MF-000005504TRJ is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Aesculap AG. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Oct 8, 2025
4039239000000415ZVPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)04046963527044
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
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 27 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Sep 23, 2009 | Still on market |
| Austria | Sep 23, 2009 | Still on market |
| Belgium | Sep 23, 2009 | Still on market |
| Bulgaria | Sep 23, 2009 | Still on market |
| Cyprus | Sep 23, 2009 | Still on market |
| Czechia | Sep 23, 2009 | Still on market |
| Denmark | Sep 23, 2009 | Still on market |
| Estonia | Sep 23, 2009 | Still on market |
| EL | Sep 23, 2009 | Still on market |
| Spain | Sep 23, 2009 | Still on market |
| Finland | Sep 23, 2009 | Still on market |
| France | Sep 23, 2009 | Still on market |
| Croatia | Sep 23, 2009 | Still on market |
| Hungary | Sep 23, 2009 | Still on market |
| Ireland | Sep 23, 2009 | Still on market |
| Italy | Sep 23, 2009 | Still on market |
| Lithuania | Sep 23, 2009 | Still on market |
| Luxembourg | Sep 23, 2009 | Still on market |
| Latvia | Sep 23, 2009 | Still on market |
| Malta | Sep 23, 2009 | Still on market |
| Netherlands | Sep 23, 2009 | Still on market |
| Poland | Sep 23, 2009 | Still on market |
| Portugal | Sep 23, 2009 | Still on market |
| Romania | Sep 23, 2009 | Still on market |
| Sweden | Sep 23, 2009 | Still on market |
| Slovenia | Sep 23, 2009 | Still on market |
| Slovakia | Sep 23, 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.
04046963527044Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
4039239000000415ZVND472RUDI 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.
L091199ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHERCertificate health across this manufacturer's portfolio.
20003GB450260622ReissuedNotified 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.
G10 010066 0438ReissuedNotified 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.
G11 010066 0437ReissuedNotified 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.
G12 010066 0441SupplementedNotified 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.
20334GB450240524IssuedNotified 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.
20333GB450240524IssuedNotified 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 →No certificate specifically references this device's Basic UDI-DI.