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

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    RGK Daily Range Wheelchairs

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776165390·Cushing Vein Retractor

    GERALD TISSUE FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896084520·GERALD TISSUE FORCEPS CROSS SERRATED TIP

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694036306·3.5mm Pilot Drill, Quick Release

    CHARGER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LIT·March 25, 2020

    PRO.DUCT CATHETER, MODEL CTH03

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

    CONMED SYSTEM 2000 ELECTROSURGICAL GENERATOR, REF: 60-8002; CONMED ESU CART, REF: 60-6120

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

    Vanguard

    FDA UDI
    Contego Medical, Inc.·00851616007453·The Vanguard IEP Peripheral Balloon Angioplasty...

    ANIMAS INSULIN CARTRIDGE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 8, 2016

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·October 15, 2008

    ADAPTA DR

    FDA Adverse Event
    Death ·MEDTRONIC MED REL, INC.·Product code NVZ·August 10, 2011

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·July 1, 2013

    3.0 RIO® ROBOTIC ARM - MICS

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·January 17, 2020

    PULSAR-18 T3 6/200/135

    FDA Adverse Event
    Malfunction ·BIOTRONIK AG·Product code NIP·December 15, 2025

    PULSAR-18 T3 5/200/135

    FDA Adverse Event
    Malfunction ·BIOTRONIK AG, BUELACH, SWITZERLAND·Product code NIP·September 19, 2024

    PULSAR-18 T3 7/200/135

    FDA Adverse Event
    Malfunction ·BIOTRONIK AG, BUELACH, SWITZERLAND·Product code NIP·February 20, 2024

    PULSAR-18 T3 6/200/135

    FDA Adverse Event
    Malfunction ·BIOTRONIK AG, BUELACH, SWITZERLAND·Product code NIP·July 16, 2021

    PULSAR-18 T3 6/200/135

    FDA Adverse Event
    Malfunction ·BIOTRONIK AG, BUELACH, SWITZERLAND·Product code NIP·November 19, 2024

    PULSAR-18 T3 6/200/135

    FDA Adverse Event
    Malfunction ·BIOTRONIK AG, BUELACH, SWITZERLAND·Product code NIP·December 11, 2024

    PULSAR-18 T3 5/200/135

    FDA Adverse Event
    Malfunction ·BIOTRONIK AG, BUELACH, SWITZERLAND·Product code NIP·April 3, 2025