BEUDAMED
    16 results · 24ms · Sources: EU EUDAMED, US FDA

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    Bone VCAR (BVCAR)

    FDA 510(k)
    FDA Class 2 ·Radiology

    Vanguard® Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00880304438194·

    SOLARC / SOLRX E-SERIES ULTRAVIOLET PHOTOTHERAPY LAMP UNIT FAMILY

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

    AIRVIEW MINI OWIE DICK TEST PACK

    FDA 510(k)
    FDA Class 2 ·General Hospital

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 24, 2017

    SERVO-S BASE UNIT

    FDA Adverse Event
    Malfunction ·MAQUET CRITICAL CARE AB·Product code CBK·December 16, 2024

    VNGD PS TIB BRG 12X63/67MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2018

    TOTAL ASR ACET IMP SIZE 52

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. - 8010379·Product code KXA·June 21, 2013

    FLO-GARD 6201 VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE (SG)·Product code FRN·October 3, 2008

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 28, 2011

    UNKNOWN PETLLA

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2018

    VAN PS CLSD INTLK FEM-RT 60

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2018

    BIOMET CC I-BEAM TRAY 63MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2018

    VNGD PS TIB BRG 12X63/67MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2018

    MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396, K173617, K181433, K183254, K192924, K203443, K213693, K213805, K220425, K231560.

    FDA Recall
    Open, Classified ·Siemens Medical Solutions USA, Inc·Product code LNH·August 28, 2025

    MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396, K173617, K181433, K183254, K192924, K203443, K213693, K213805, K220425, K231560.

    FDA Enforcement
    Class I ·Ongoing·Siemens Medical Solutions USA, Inc·October 8, 2025