- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Feb 15, 2023
8052705961551717518185E2AC 180 B DA 600 PZ is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by SA.GE srl. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
180527059601888052705961551717518185E2AC 180 B DA 600 PZ(01)18052705960188
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.
V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER2 warnings recorded — scroll inside the panel to see all entries.
CW009CW010No certificate specifically references this device's Basic UDI-DI.
Primary placement in Italy; available across 1 country total.
Placed on the market in Italy; per-country availability dates not published.
IT-MF-000030827No 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.