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EUDAMED last updated this device on May 25, 2026
8033895W01030708C061XFRSCHIFF REAGENT ACC. FEULGEN - 500 ML is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Diapath S.p.A. società a socio unico. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
08033895007528C0612IT-MF-000027016(01)08033895007528
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
2 warnings recorded — scroll inside the panel to see all entries.
CW010CW999Sterile
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 Italy; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | — | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
W01030708STAIN SOLUTIONS (HISTOLOGY/CYTOLOGY)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.
8033895W01030705SafCap2XOn the marketSAFECAPSULE – FORMALIN AND MARKER (7ML) 35 PCS8033895W01030705SafCap2XOn the marketSAFECAPSULE PROSTATE BIOPSY KIT8033895W01030705SfCp100RQOn the marketSCHIFF REAGENT ACC. HOTCHKISS - MCMANUS - 1 LT8033895W01030708C062XFUOn the marketSERIGRAPHED DISPOSABLE TUB XL (3000 ML) - 120 PCS8033895W05020104ContMonE6On the marketSICURA PRE-FILLED CONTAINER 10% NEUTRAL BUFFERED FORMALIN RTU PRESS ON CAP 1 LT (700 ML) 40 PCS x 01 PACK8033895W01030705SicFor6XOn the marketNo 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.