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Agilent Technologies Denmark ApS

DK Last updated 23 Oct 2026

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Devices
0
Registries
FDA
FDA recalls
33 ongoing

Catalogue0

No devices listed yet from this manufacturer.

FDA recalls3

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.

  • 2025

    • 11 Aug 2025 Z-2563-2025 Class II Ongoing Their is the potential for weak staining which may result in false negative CD20 identification.
    • 11 Aug 2025 Z-2564-2025 Class II Ongoing Their is the potential for weak staining which may result in false negative CD20 identification.
    • 11 Aug 2025 Z-2565-2025 Class II Ongoing Their is the potential for weak staining which may result in false negative CD20 identification.

Information

Country
DK
Address
42 PRODUKTIONSVEJ, GLOSTRUP Hovedstaden
FDA FEI number
3002806778