BEUDAMED
    107 results · 26ms · Sources: EU EUDAMED, US FDA

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    Spectralis HRA+OCT and variants

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668114247·VECTIS 2-HOLE 4MM 25GA (PK/10)

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112878·CORNEAL TREPHINE BLADE6.5MM

    DJO SURGICAL

    FDA UDI
    Encore Medical, L.P.·00190446327264·SPECIAL, EMPOWR 2° VARUS/VALGUS TIBIAL CUT BLOCK

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306823879·Mead Mallet With Plastic Disks, 230 grams, 18.5cm

    MULTI HOLE 12 INFILTRATION

    FDA UDI
    The Wells Johnson Company·B458201252000·Cannula, Multi-Hole 12 Infiltration, specify le...

    BLOOD-PRESSURE METER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MAXHEALTH WHEELCHAIR, MODEL HE-8631, HE-8621, HE-8651

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    T:SLIM G5 SYSTEM

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code OYC·March 20, 2018

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 29, 2025

    GMK-REVISION 02.07.0685L REVISION FIXED TIBIAL TRAY CEMENTED SIZE 5 L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·January 25, 2023

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·October 27, 2014

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 11, 2011

    WALLFLEX? DUODENAL

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code MUM·July 2, 2013

    BIOMET

    FDA Adverse Event
    Injury ·BIOMET·Product code JDI·September 21, 2018

    RESTORE

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·September 7, 2012

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·September 2, 2022

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·September 2, 2022

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·September 2, 2022

    CHECK-IT

    FDA Adverse Event
    Malfunction ·LUCIRA HEALTH, INC.·Product code QJR·September 2, 2022