- Role
- Country
- Date of registration
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EUDAMED last updated this device on Jun 11, 2026
8033895W01030705QCPNGYNKFCYTOPATH-FIXATIVE SOLUTION 60 ML (20 ML) 25 PCS x 1 PACK 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.
IT-MF-000027016(01)08033895049207
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 |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
08033895049207Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
8033895W01030705QCPNGYNKFCP204UDI 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.
W01030705FIXING REAGENTS (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 →No certificate specifically references this device's Basic UDI-DI.
8033895W01030708CP50XNAOn the marketCYTOPATH DISC 12 MM8033895W02029099CPD2ZOn the marketCYTOPATH DISC 6 MM8033895W02029099CPD2ZOn the marketDIACUT ULTRA PLUS 50 PZ8033895W0202059085055BBOn the marketDIAPRINT SLIDE WHITE - 2000 PCS8033895W0503900201GP090NLOn the marketDIAPRINT TISSUE CASSETTES - WHITE 1000 PCS8033895W05030501GP070X9YOn 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.