BEUDAMED
    327 results · 30ms · Sources: EU EUDAMED, US FDA

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    STRETCH VINYL EXAMINATION GLOVE POWDER FREE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    REPICCI II RESURFACING KNEE SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304002401·

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112953·CORNEAL TREPHINE BLADE8.5MM

    ATEC A.R.M.

    FDA UDI
    ALPHATEC SPINE, INC.·00190376532448·MECH A-ARM CONTROL HARNESS

    Viceroy

    FDA UDI
    DIOMEDICAL CO.,LTD.·08800113904712·VICEROY Rod - 5.5 (D)5.5x(L)160mm

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523129904·Reduction Screw Implant Caddy Lid for 6.0 mm Rod

    ZEUS-L

    FDA UDI
    SPINAL ELEMENTS·00840916141103·ZEUS® LLIF 10mm x 21mm x 60mm x 07° TRIAL

    SPIRA®-A Integrated

    FDA UDI
    CAMBER SPINE TECHNOLOGIES, LLC·B030SAZ1021600·SPIRA®-A Integrated,Trial, 32x38mm, 30° Lordoti...

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197058544·Button-end Probe Ø1mm, ...

    ZEUS-L

    FDA UDI
    SPINAL ELEMENTS·00840916134334·ZEUS®-L, Lateral Lumber Interbody Fusion Device...

    Tibial Trial Tray 5

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215056575·

    ZZOMA POSITIONAL SLEEPER MODEL 001

    FDA 510(k)
    FDA Class 2 ·Dental

    COMPCORE AF COMPOSITE CORE BUILD-UP MATERIAL, MODEL 3001408

    FDA 510(k)
    FDA Class 2 ·Dental

    Dukal

    FDA UDI
    Dukal LLC·10665973013760·Clinisorb Non-Woven Sponges 2" x 2" 4-Ply, Non-...

    IMP TM 4.7MM MTX FULL, 11.5MM

    FDA Adverse Event
    Injury ·ZIMMER DENTAL·Product code DZE·November 25, 2022

    IMP TM 4.7MM MTX FULL, 10

    FDA Adverse Event
    Injury ·ZIMVIE US CORP LLC·Product code DZE·April 23, 2026

    IMP TM 4.7MM MTX FULL, 10

    FDA Adverse Event
    Injury ·ZIMVIE US CORP LLC·Product code DZE·April 23, 2026

    9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 3, 2013

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·September 19, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 20, 2011