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Agfa Gevaert N.V.

BE Last updated 23 Oct 2026

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Devices
0
Registries
FDA
FDA recalls
1

Catalogue0

No devices listed yet from this manufacturer.

FDA recalls1

Recalls this firm reported to the FDA. Device pages show the recalls that name the device or the 510(k)/PMA it was cleared under.

  • 2018

    • 4 Dec 2018 Z-0692-2019 Class II Terminated After an upgrade of the software of the Overhead Tube Crane, there were isolated cases in which the Overhead Tube Crane movement does not stop when the movement button is released. Instead of stopping while the movement button is released, the Tube Head Crane moves to the intended position.

Information

Country
BE
Address
27 Septestraat, Mortsel Antwerpen
FDA FEI number
3002809633