- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Jul 24, 2025
80322485100089B-BLOCK.PRO G20X32 PUR RNL is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Delta Med SPA. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
080322485127648032248510008958044432200550(01)08032248512764
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.
C01010103PERIPHERAL I.V. CATHETERS, WITH INTEGRATED EXTENSIONS5 warnings recorded — scroll inside the panel to see all entries.
CW011CW001CW009CW007CW010No certificate specifically references this device's Basic UDI-DI.
Primary placement in Italy; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Still on market |
IT-MF-000027962No 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.