BEUDAMED
    345 results · 38ms · Sources: EU EUDAMED, US FDA

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    MODULAR DUAL MOBILITY LINER, X3 ACETABULAR INSERT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PMT CORPORATION - STEREOTACTIC

    FDA UDI
    PMT CORPORATION·00650551003496·Globus Excelsius GPS Driver Bushing for 2.7 / 3...

    MILLER BONE RASPATORY

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896052413·MILLER BONE RASPATORY DOUBLE ENDED SINGLE-SIDED...

    CapSure® Spine System

    FDA UDI
    Spine Wave, Inc.·10840642129878·PS3 Tap, 5.5mm, NAV-M

    RS NITRILSTST MEDICAL EXAMINATION GLOVES, POWDERED (NON STERILE) BLUE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    SUDOSCAN

    FDA 510(k)
    FDA Class 2 ·Neurology

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·September 21, 2022

    KALTOSTAT

    FDA Adverse Event
    Malfunction ·CONVATEC LTD·Product code NAC·September 20, 2022

    ACCU-CHEK ® AVIVA PLUS TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·May 9, 2013

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·September 19, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·May 25, 2011

    CS100 INTRA-AORTIC BALLOON PUMP, ENGLISH, 220V

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·January 11, 2022

    CARDIOSAVE HYBRID, TYPE I PLUG

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·December 21, 2021

    AMISTEM H SIZE 1 LAT

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·November 8, 2013

    CS100 INTRA-AORTIC BALLOON PUMP, CHINESE, 220V

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·September 13, 2021

    INTERGARD CARDIOROOT

    FDA Adverse Event
    Malfunction ·INTERVASCULAR SAS·Product code DSY·April 13, 2026

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code HRS·October 24, 2015

    INTERGARD WOVEN AORTIC ARCH

    FDA Adverse Event
    Malfunction ·INTERVASCULAR SAS·Product code DSY·April 20, 2026

    INTERGARD WOVEN

    FDA Adverse Event
    Malfunction ·INTERVASCULAR SAS·Product code DSY·April 20, 2026

    CS300 INTRA-AORTIC BALLOON PUMP, ENGLISH, 220V

    FDA Adverse Event
    Malfunction ·DATASCOPE CORP. - MAHWAH·Product code DSP·June 2, 2022