- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 26, 2026
69301978202101s03801F71693019788228269301978202101s03801F7ZRSPSE-10-BLUE(01)16930197882282
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.
A070501CAPS OR OBTURATORS, NON-PERFORABLE3 warnings recorded — scroll inside the panel to see all entries.
CW010CW018CW030No certificate specifically references this device's Basic UDI-DI.
Primary placement in Netherlands; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | Still on market |
CN-MF-000005652No 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.