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EUDAMED last updated this device on Jun 2, 2026
426246385PG259V2513-221 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Meditec Source GmbH & Co. KG. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
04262463851704426246385PG259V2513-221(01)04262463851704
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.
L0922ORTHOPAEDIC SURGERY GUIDES, REUSABLENo certificate specifically references this device's Basic UDI-DI.
Primary placement in Germany; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Still on market |
DE-MF-000006490No 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.