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EUDAMED last updated this device on May 29, 2026
69520627J034LD0695206277405169520627J034LDCFRA1ST-10(01)06952062774051
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0105099099VIROLOGY - RT & POC - OTHER3 warnings recorded — scroll inside the panel to see all entries.
CW010CW009CW007No certificate specifically references this device's Basic UDI-DI.
Primary placement in Germany; available across 32 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Nov 4, 2025 | Mar 21, 2030 |
| Austria | Nov 4, 2025 | Mar 21, 2030 |
| Belgium | Nov 4, 2025 | Mar 21, 2030 |
| Bulgaria | Nov 4, 2025 | Mar 21, 2030 |
| Cyprus | Nov 4, 2025 | Mar 21, 2030 |
| Czechia | Nov 4, 2025 | Mar 21, 2030 |
| Denmark | Nov 4, 2025 | Mar 21, 2030 |
| Estonia | Nov 4, 2025 | Mar 21, 2030 |
| EL | Nov 4, 2025 | Mar 21, 2030 |
| Spain | Nov 4, 2025 | Mar 21, 2030 |
| Finland | Nov 4, 2025 | Mar 21, 2030 |
| France | Nov 4, 2025 | Mar 21, 2030 |
| Croatia | Nov 4, 2025 | Mar 21, 2030 |
| Hungary | Nov 4, 2025 | Mar 21, 2030 |
| Ireland | Nov 4, 2025 | Mar 21, 2030 |
| Iceland | Nov 4, 2025 | Mar 21, 2030 |
| Italy | Nov 4, 2025 | Mar 21, 2030 |
| Liechtenstein | Nov 4, 2025 | Mar 21, 2030 |
| Lithuania | Nov 4, 2025 | Mar 21, 2030 |
| Luxembourg | Nov 4, 2025 | Mar 21, 2030 |
| Latvia | Nov 4, 2025 | Mar 21, 2030 |
| Malta | Nov 4, 2025 | Mar 21, 2030 |
| Netherlands | Nov 4, 2025 | Mar 21, 2030 |
| Norway | Nov 4, 2025 | Mar 21, 2030 |
| Poland | Nov 4, 2025 | Mar 21, 2030 |
| Portugal | Nov 4, 2025 | Mar 21, 2030 |
| Romania | Nov 4, 2025 | Mar 21, 2030 |
| Sweden | Nov 4, 2025 | Mar 21, 2030 |
| Slovenia | Nov 4, 2025 | Mar 21, 2030 |
| Slovakia | Nov 4, 2025 | Mar 21, 2030 |
| Türkiye | Nov 4, 2025 | Mar 21, 2030 |
| XI | Nov 4, 2025 | Mar 21, 2030 |
CN-MF-000018785No 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.69520627J161LMOn the marketCOVID-19 & Influenza A+B & RSV & ADV & HMPV Antigen Combo Test Kit (LFA)69520627J161LMOn the marketCOVID-19 & Influenza A+B & RSV & ADV & HMPV Antigen Combo Test Kit (LFA)69520627J161LMOn the marketCOVID-19 & Influenza A+B & RSV & ADV & HMPV Antigen Combo Test Kit (LFA)69520627J161LMOn the marketInfluenza A+B & COVID-19 (SARS-CoV-2) Antigen Test Kit (Colloidal Gold)69520627J017LDOn the market