- Organization name
- UDI-DI code
- Reference / catalog number
DE-MF-000010123004794 MR2Assistent Blutlanzetten is an MDD-legacy medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by KERN LIEBERS Schwabmünchen GmbH. Placed on the EU market in Austria. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Aug 12, 2026
B-112069214110Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
112069214110
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA / IFA support is coming.
2 warnings 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 Austria; available across 31 countries total.
| Country | On market since | Until |
|---|---|---|
| AustriaPrimary placement | — | Still on market |
| Bulgaria | Jan 1, 2020 | Dec 31, 2028 |
| Cyprus | Jan 1, 2020 | Dec 31, 2028 |
| Czechia | Jan 1, 2020 | Dec 31, 2028 |
| Germany | Jan 1, 2020 | Dec 31, 2028 |
| Denmark | Jan 1, 2020 | Dec 31, 2028 |
| Estonia | Jan 1, 2020 | Dec 31, 2028 |
| EL | Jan 1, 2020 | Dec 31, 2028 |
| Spain | Jan 1, 2020 | Dec 31, 2028 |
| Finland | Jan 1, 2020 | Dec 31, 2028 |
| France | Jan 1, 2020 | Dec 31, 2028 |
| Croatia | Jan 1, 2020 | Dec 31, 2028 |
| Hungary | Jan 1, 2020 | Dec 31, 2028 |
| Ireland | Jan 1, 2020 | Dec 31, 2028 |
| Iceland | Jan 1, 2020 | Dec 31, 2028 |
| Italy | Jan 1, 2020 | Dec 31, 2028 |
| Liechtenstein | Jan 1, 2020 | Dec 31, 2028 |
| Lithuania | Jan 1, 2020 | Dec 31, 2028 |
| Luxembourg | Jan 1, 2020 | Dec 31, 2028 |
| Latvia | Jan 1, 2020 | Dec 31, 2028 |
| Malta | Jan 1, 2020 | Dec 31, 2028 |
| Netherlands | Jan 1, 2020 | Dec 31, 2028 |
| Norway | Jan 1, 2020 | Dec 31, 2028 |
| Poland | Jan 1, 2020 | Dec 31, 2028 |
| Portugal | Jan 1, 2020 | Dec 31, 2028 |
| Romania | Jan 1, 2020 | Dec 31, 2028 |
| Sweden | Jan 1, 2020 | Dec 31, 2028 |
| Slovenia | Jan 1, 2020 | Dec 31, 2028 |
| Slovakia | Jan 1, 2020 | Dec 31, 2028 |
| Türkiye | Jan 1, 2020 | Dec 31, 2028 |
| XI | Jan 1, 2020 | 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.
112069214110Basic 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-112069214110Schlüsselnummer 301UDI 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.
V010402LANCETS WITHOUT SAFETY SYSTEMS, SINGLE-USEB-112069227607On the marketAllergy Therapeutics LancetB-112069246046On the marketAMEFA medimex BlutlanzettenB-112069221866On the marketAssistent BlutlanzettenB-112069214110On the marketbetamedAllergy LancetsB-112069257287On the marketHAL Allergy Prick lancetsB-112069230754On the marketNo 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.No certificate specifically references this device's Basic UDI-DI.