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EUDAMED last updated this device on Aug 8, 2022
87193275323DSA3500HRDSA3500 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Dental International. Placed on the EU market in Netherlands. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0871932753228787193275323DSA3500HRDSA3500(01)08719327532287
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 - OTHERNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Netherlands; available across 11 countries total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | Aug 8, 2022 | Jan 1, 2040 |
| Austria | Aug 8, 2022 | Jan 1, 2040 |
| Belgium | Aug 8, 2022 | Jan 1, 2040 |
| Germany | Aug 8, 2022 | Jan 1, 2040 |
| Spain | Aug 8, 2022 | Jan 1, 2040 |
| France | Aug 8, 2022 | Jan 1, 2040 |
| Ireland | Aug 8, 2022 | Jan 1, 2040 |
| Luxembourg | Aug 8, 2022 | Jan 1, 2040 |
| Portugal | Aug 8, 2022 | Jan 1, 2040 |
| Sweden | Aug 8, 2022 | Jan 1, 2040 |
| XI | Aug 8, 2022 | Jan 1, 2040 |
NL-MF-000010964No 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.