- Organization name
- UDI-DI code
- Reference / catalog number
GB-MF-000029354RPR Carbon Antigen is an IVDD-legacy in vitro diagnostic registered in EUDAMED. It is classified as IVDD — General. Manufactured by Lorne Laboratories Ltd. Placed on the EU market in Malta. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Sep 7, 2026
B-05060168051264Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)05060168051264
1 warning 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.
Primary placement in Malta; available across 25 countries total.
| Country | On market since | Until |
|---|---|---|
| MaltaPrimary placement | Jun 17, 2004 | Still on market |
| Austria | Jun 17, 2004 | Still on market |
| Belgium | Jun 17, 2004 | Still on market |
| Bulgaria | Jun 17, 2004 | Still on market |
| Cyprus | Jun 17, 2004 | Still on market |
| Czechia | Jun 17, 2004 | Still on market |
| Germany | Jun 17, 2004 | Still on market |
| Denmark | Jun 17, 2004 | Still on market |
| Estonia | Jun 17, 2004 | Still on market |
| EL | Jun 17, 2004 | Still on market |
| Spain | Jun 17, 2004 | Still on market |
| France | Jun 17, 2004 | Still on market |
| Hungary | Jun 17, 2004 | Still on market |
| Ireland | Jun 17, 2004 | Still on market |
| Italy | Jun 17, 2004 | Still on market |
| Lithuania | Jun 17, 2004 | Still on market |
| Latvia | Jun 17, 2004 | Still on market |
| Netherlands | Jun 17, 2004 | Still on market |
| Poland | Jun 17, 2004 | Still on market |
| Portugal | Jun 17, 2004 | Still on market |
| Romania | Jun 17, 2004 | Still on market |
| Slovenia | Jun 17, 2004 | Still on market |
| Slovakia | Jun 17, 2004 | Still on market |
| Türkiye | Jun 17, 2004 | Still on market |
| XI | Jun 17, 2004 | 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.
05060168051264Basic 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-05060168051264045005AUDI 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.
W0105010301SYPHILIS ANTIGEN DETECTIONNo 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.