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US-MF-000040030PRAS CCFA is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Anaerobe Systems. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Jul 22, 2025
081004890ANAEROBEDTPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)00810048900121
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 Netherlands; available across 32 countries total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | Jul 21, 2025 | Still on market |
| Austria | Jul 21, 2025 | Still on market |
| Belgium | Jul 21, 2025 | Still on market |
| Bulgaria | Jul 21, 2025 | Still on market |
| Cyprus | Jul 21, 2025 | Still on market |
| Czechia | Jul 21, 2025 | Still on market |
| Germany | Jul 21, 2025 | Still on market |
| Denmark | Jul 21, 2025 | Still on market |
| Estonia | Jul 21, 2025 | Still on market |
| EL | Jul 21, 2025 | Still on market |
| Spain | Jul 21, 2025 | Still on market |
| Finland | Jul 21, 2025 | Still on market |
| France | Jul 21, 2025 | Still on market |
| Croatia | Jul 21, 2025 | Still on market |
| Hungary | Jul 21, 2025 | Still on market |
| Ireland | Jul 21, 2025 | Still on market |
| Iceland | Jul 21, 2025 | Still on market |
| Italy | Jul 21, 2025 | Still on market |
| Liechtenstein | Jul 21, 2025 | Still on market |
| Lithuania | Jul 21, 2025 | Still on market |
| Luxembourg | Jul 21, 2025 | Still on market |
| Latvia | Jul 21, 2025 | Still on market |
| Malta | Jul 21, 2025 | Still on market |
| Norway | Jul 21, 2025 | Still on market |
| Poland | Jul 21, 2025 | Still on market |
| Portugal | Jul 21, 2025 | Still on market |
| Romania | Jul 21, 2025 | Still on market |
| Sweden | Jul 21, 2025 | Still on market |
| Slovenia | Jul 21, 2025 | Still on market |
| Slovakia | Jul 21, 2025 | Still on market |
| Türkiye | Jul 21, 2025 | Still on market |
| XI | Jul 21, 2025 | 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.
00810048900121Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
081004890ANAEROBEDTAS-213UDI 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.
W0104010405NON-CHROMOGENIC MEDIA (PLATES)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.081004890ANAEROBEDTOn the marketPRAS CAMPY081004890ANAEROBEDTOn the marketPRAS CBA (4 plates /pkg)081004890ANAEROBEDTOn the marketPRAS CCFA-HT (1 plate)081004890ANAEROBEDTOn the marketPRAS CCFA-L (1 plate)081004890ANAEROBEDTOn the marketPRAS CDC (4 plates /pkg)081004890ANAEROBEDTOn the marketNo certificate specifically references this device's Basic UDI-DI.