- Role
- Country
- Date of registration
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EUDAMED last updated this device on May 29, 2026
4035282REMAShaverBladeS28DE-MF-000011317No 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.Primary placement in Germany; available across 10 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Jul 25, 2025 | Still on market |
| Bulgaria | Jul 25, 2025 | Still on market |
| Cyprus | Jul 25, 2025 | Still on market |
| EL | Jul 25, 2025 | Still on market |
| Spain | Jul 25, 2025 | Still on market |
| France | Jul 25, 2025 | Still on market |
| Netherlands | Jul 25, 2025 | Still on market |
| Poland | Jul 25, 2025 | Still on market |
| Portugal | Jul 25, 2025 | Still on market |
| Romania | Jul 25, 2025 | Still on market |
(01)04035282355797
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.
K030203ARTHROSCOPY BLADES, SINGLE-USE