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EUDAMED last updated this device on May 25, 2026
4260484130006TT0051 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Greten Prismaflex GmbH. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
042604841300684260484130006TT0051(01)04260484130068
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.
Q0299OPHTHALMIC DEVICES - OTHERNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Germany; available across 10 countries total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Jan 2, 2013 | Still on market |
| Austria | May 25, 2026 | Still on market |
| Belgium | May 25, 2026 | Still on market |
| Denmark | May 25, 2026 | Still on market |
| Finland | May 25, 2026 | Still on market |
| France | May 25, 2026 | Still on market |
| Italy | May 25, 2026 | Still on market |
| Netherlands | May 25, 2026 | Still on market |
| Norway | May 25, 2026 | Still on market |
| Sweden | May 25, 2026 | Still on market |
DE-MF-000026567No 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.