- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on May 27, 2026
5060599400002RNXCup Reader is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Rapid Labs Ltd. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
5061109830306RL-CD-1A5061109830306
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA / IFA support is coming.
European Medical Device Nomenclature — the EU product classification assigned to this device.
W02010701URINALYSIS (UR) - LABORATORY ANALYSERS- INSTRUMENTSPrimary placement in Italy; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Feb 22, 2025 | Still on market |
GB-MF-000026335Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
View in glossary →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.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →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.
View in glossary →Primary 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.
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.5060599401039XMOn the marketCryptosporidium Ag and Giardia Lamblia Ag Combo Test Device-FecesB-D-FICRYGLD106YOn the marketCryptosporidium Ag and Giardia Lamblia Ag Combo Test Device-FecesB-D-FICRYGLD257DOn the marketCup Reader5060599401040X6On the marketDengue Combo Rapid Test DeviceB-D-DAGMD20Q6On the marketEnterovirus 71 Ag Test Device-FecesB-D-FIEV71AGD25QHOn the market