- Organization name
- UDI-DI code
- Reference / catalog number
FR-MF-000007902RAL Diff-Quik™ solution I is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by RAL Diagnostics. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on May 7, 2026
376017719720570KXPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)03760177194540
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
6 warnings 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 France; available across 32 countries total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Aug 8, 2017 | Dec 31, 2039 |
| Austria | Aug 8, 2017 | Dec 31, 2039 |
| Belgium | Aug 8, 2017 | Dec 31, 2039 |
| Bulgaria | Aug 8, 2017 | Dec 31, 2039 |
| Cyprus | Aug 8, 2017 | Dec 31, 2039 |
| Czechia | Aug 8, 2017 | Dec 31, 2039 |
| Germany | Aug 8, 2017 | Dec 31, 2039 |
| Denmark | Aug 8, 2017 | Dec 31, 2039 |
| Estonia | Aug 8, 2017 | Dec 31, 2039 |
| EL | Aug 8, 2017 | Dec 31, 2039 |
| Spain | Aug 8, 2017 | Dec 31, 2039 |
| Finland | Aug 8, 2017 | Dec 31, 2039 |
| Croatia | Aug 8, 2017 | Dec 31, 2039 |
| Hungary | Aug 8, 2017 | Dec 31, 2039 |
| Ireland | Aug 8, 2017 | Dec 31, 2039 |
| Iceland | Aug 8, 2017 | Dec 31, 2039 |
| Italy | Aug 8, 2017 | Dec 31, 2039 |
| Liechtenstein | Aug 8, 2017 | Dec 31, 2039 |
| Lithuania | Aug 8, 2017 | Dec 31, 2039 |
| Luxembourg | Aug 8, 2017 | Dec 31, 2039 |
| Latvia | Aug 8, 2017 | Dec 31, 2039 |
| Malta | Aug 8, 2017 | Dec 31, 2039 |
| Netherlands | Aug 8, 2017 | Dec 31, 2039 |
| Norway | Aug 8, 2017 | Dec 31, 2039 |
| Poland | Aug 8, 2017 | Dec 31, 2039 |
| Portugal | Aug 8, 2017 | Dec 31, 2039 |
| Romania | Aug 8, 2017 | Dec 31, 2039 |
| Sweden | Aug 8, 2017 | Dec 31, 2039 |
| Slovenia | Aug 8, 2017 | Dec 31, 2039 |
| Slovakia | Aug 8, 2017 | Dec 31, 2039 |
| Türkiye | Aug 8, 2017 | Dec 31, 2039 |
| XI | Aug 8, 2017 | Dec 31, 2039 |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
03760177194540Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
376017719720570KX720570-2500UDI 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.
W0103010399HAEMATOLOGY STAINS FOR MICROSCOPY - OTHER376017719300012GEOn the marketRAL Diff-Quik™ Fixative solution376017719720560KUOn the marketRAL Diff-Quik™ Fixative solution376017719720560KUOn the marketRAL Diff-Quik™ solution I376017719720570KXOn the marketRAL Diff-Quik™ solution II376017719720580L2On the marketRAL Diff-Quik™ solution II376017719720580L2On the marketNo 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.