BEUDAMED
    220 results · 25ms · Sources: EU EUDAMED, US FDA

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    GRANDTEC

    FDA 510(k)
    FDA Class 2 ·Dental

    JOBST Bella Strong

    FDA UDI
    BSN MEDICAL, INC.·00035664009915·BELLA STRONG 20-30 MM HG ARMSLEEVE KNIT WELT SI...

    COOLTOUCH II

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    PROTEGE SELF-EXPANDING NITINOL STENT WITH STARPORT DELIVERY TECHNOLOGY

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    GMK-REVISION FEMUR REVISION PS SIZE 6 RIGHT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·April 12, 2017

    GMK-HINGE FIXED TIBIAL TRAY SIZE 3 R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code KRO·August 28, 2019

    GMK HINGE FEMUR SIZE 5 RIGHT

    FDA Adverse Event
    Injury ·MEDACTA INTERNAIONAL SA·Product code KRO·August 21, 2014

    GMK-REVISION FIXED TIBIAL TRAY CEMENTED SIZE 3 RIGHT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·October 25, 2017

    GMK-REVISION FEMUR REVISION PS SIZE 3

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·June 19, 2019

    KYPHX HV-R BONE CEMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·February 25, 2020

    GMK HINGE FEMUR SIZE 2 RIGHT

    FDA Adverse Event
    Injury ·Product code KRO·September 12, 2014

    GMK REVISION TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 29, 2025

    GMK-REVISION FEMUR REVISION PS SIZE 6 L

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·September 6, 2018

    GMK-SPHERE FEMORAL COMPONENT CEMENTED SIZE 3+ RIGHT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·October 12, 2017

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Malfunction ·WAVELIGHT GMBH·Product code LZS·April 30, 2013

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·September 19, 2014

    RESTORE RECHARGABLE NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·May 20, 2011

    KYPHON XPEDE BONE CEMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·November 6, 2019

    KYPHON XPEDE BONE CEMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NDN·July 30, 2019

    GMK REVISION TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·October 15, 2025