- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 25, 2026
697022652107FSEXTesia is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Curatia Medical Limited. Placed on the EU market in Estonia. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
06941358012243697022652107FS2IS041635SJI(01)06941358012243
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.
C0504ARTERIAL INTRODUCTION SETS1 warning recorded — scroll inside the panel to see all entries.
CW009No certificate specifically references this device's Basic UDI-DI.
Primary placement in Estonia; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| EstoniaPrimary placement | Still on market |
CN-MF-000015976No 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.