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

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    AMES DCA 2000TM ANALYZER AND REAGENT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Hematology

    Edge™ Diamond ND016-5F Needle

    FDA UDI
    CLINICIAN'S CHOICE DENTAL PRODUCTS, INC.·07540172002554·Diamond dental bur, reusable

    REVELATION DIAMOND

    FDA UDI
    Ss White Burs, Inc.·D6909116252·REVELATION DIAMOND 368-020C - 5 PACK

    VASOCOR VASCULAR DIAGNOSTIC CENTER (MODEL 300)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Persona Revision Knee System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FEMORAL POSTERIOR AUGMENT CEMENTED

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 2, 2022

    STEM EXTENSION STRAIGHT SPLINED UNCEMENTED

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 2, 2022

    FEMORAL DISTAL AUGMENT CEMENTED

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 2, 2022

    TIBIAL AUGMENT CEMENTED HALF BLOCK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 2, 2022

    FEMORAL DISTAL AUGMENT CEMENTED

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·August 17, 2022

    TIBIAL AUGMENT CEMENTED HALF BLOCK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·August 17, 2022

    SEE H10 NARRATIVE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·May 16, 2023

    SEE H10 NARRATIVE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·May 16, 2023

    TIBIA FIXED CEMENTED LEFT SIZE D STEM EXTENSION

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·May 16, 2023

    TIBIAL AUGMENT CEMENTED HALF BLOCK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·August 17, 2022

    STYLE 410 COHESIVE SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·August 29, 2019

    LIFESTART VASCULAR STENT SYSTEM

    FDA Adverse Event
    Injury ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIO·May 27, 2014

    UNKNOWN DEPUY ASR HIP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·November 29, 2010

    LIGASURE IMPACT

    FDA Adverse Event
    Malfunction ·VALLEYLAB·Product code GEI·August 29, 2007

    SEE H10

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDG·June 4, 2018