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DE-MF-000008156Anti-A1 for card method Lectin (Dolichos biflorus) is an IVDD-legacy in vitro diagnostic registered in EUDAMED. It is classified as IVDD — General. Manufactured by ANTITOXIN GmbH. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Jul 3, 2026
B-04250861815404Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)04250861815404
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.
Primary placement in Germany; available across 14 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Jan 1, 2019 | Still on market |
| Austria | Jan 1, 2019 | Still on market |
| Denmark | Jan 1, 2019 | Still on market |
| EL | Jan 1, 2019 | Still on market |
| Spain | Jan 1, 2019 | Still on market |
| France | Jan 1, 2019 | Still on market |
| Ireland | Jan 1, 2019 | Still on market |
| Italy | Jan 1, 2019 | Still on market |
| Norway | Jan 1, 2019 | Still on market |
| Portugal | Jan 1, 2019 | Still on market |
| Sweden | Jan 1, 2019 | Still on market |
| Slovenia | Jan 1, 2019 | Still on market |
| Türkiye | Jan 1, 2019 | Still on market |
| XI | Jan 1, 2019 | 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.
04250861815404Basic 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-0425086181540404.235-03UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
IVDR risk classes
IVDR risk classes rank in-vitro diagnostic devices from lowest risk (Class A) to highest (Class D), based on the patient and public-health risk of a wrong result.
European Medical Device Nomenclature — the EU product classification assigned to this device.
W01030399IMMUNOHAEMATOLOGY (BLOOD GROUPING) TESTS - OTHERNo 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.B-04250861821283On the marketAHG serum blendB-04250861805337On the marketAnti-A monoclonal, IgM clone: Birma-1B-04250861800110On the marketAnti-AB monoclonal, IgM clones: ES-15, ES-4B-04250861800318On the marketAnti-B monoclonal, IgM clone: LB-2B-04250861800219On the marketAnti-C monoclonal, human IgM clone: MS-273B-04250861801315On the market