BEUDAMED
    15 results · 22ms · Sources: EU EUDAMED, US FDA

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    Electric wheelchair (Model: S7012)

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    FUSION MEDICAL RING LOCK SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EECP THERAPY SYSTEM MODEL TS3 WITH PULSE OXIMETRY AND ENHANCED EXTERNAL COUNTERPULSATION EECP MC-2 EXTERNAL COUNTER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EECP THERAPY SYSTEM, MODEL TS3

    FDA Adverse Event
    Injury ·VASOMEDICAL, INC.·Product code DRN·December 30, 2002

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

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

    FLO-GARD 6201 VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE (SG)·Product code FRN·October 20, 2008

    RESTORE PRIME ADVANCED

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·August 8, 2011

    PROXIMATE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GDW·May 31, 2013

    UNKNOWN KNEE FEMORAL

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·October 1, 2019

    UNK - CONSTRUCTS: LCP

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HRS·August 13, 2021

    UNKNOWN HIP FEMORAL STEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JDI·October 1, 2019

    UNKNOWN KNEE TIBIAL TRAY

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·October 1, 2019

    UNKNOWN KNEE TIBIAL INSERT

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·October 1, 2019

    TALENT THORACIC STENT GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC CARDIOVASCULAR·Product code MIH·August 18, 2010

    Toshiba Infinix-i X-Ray System. A radiographic and fluoroscopic x-ray system for use in diagnostic and angiographic procedures.

    FDA Enforcement
    Class II ·Terminated·Toshiba American Medical Systems Inc·April 3, 2013