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EUDAMED last updated this device on May 25, 2023
57000022502PDRHPD-100 is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by PRO Devices A/S. Placed on the EU market in Denmark. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
05700002250209PD-100DK-MF-000000962(01)05700002250209
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.
Primary placement in Denmark; available across 11 countries total.
| Country | On market since | Until |
|---|---|---|
| DenmarkPrimary placement | May 1, 2020 | Still on market |
| Austria | Nov 1, 2024 | Still on market |
| Czechia | Nov 1, 2024 | Still on market |
| Germany | Dec 1, 2022 | Still on market |
| Estonia | Nov 1, 2024 | Still on market |
| Hungary | Nov 1, 2024 | Still on market |
| Lithuania | Nov 1, 2024 | Still on market |
| Latvia | Nov 1, 2024 | Still on market |
| Poland | Nov 1, 2024 | Still on market |
| Sweden | May 1, 2020 | Still on market |
| Slovenia | Nov 1, 2024 | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
W02030199ANTIBIOTIC SUSCEPTIBILITY ANALYSERS - OTHERPrimary 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 →This device is not currently linked to any other device.
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.