- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 30, 2026
69317478SP000021NW0693174783654369317478SP000021NW100005(01)06931747836543
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.
T0202SURGICAL PROCEDURAL KITS (EXCLUDING SURGICAL INSTRUMENT KITS)2 warnings recorded — scroll inside the panel to see all entries.
CW009CW007No certificate specifically references this device's Basic UDI-DI.
Primary placement in Germany; available across 2 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Oct 29, 2023 | Dec 31, 2099 |
| Czechia | Oct 29, 2023 | Dec 31, 2099 |
CN-MF-000009427No 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.