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

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    KOMET XK-95 PERFORATOR MOTOR (MI-102)

    FDA 510(k)
    FDA Class 2 ·Neurology

    Pro Harrington Blade

    FDA UDI
    KOROS U.S.A., INC.·10840199542670·Pro Harrington (Sweetheart) Blade Large 2-1/2 x 5"

    102 P37,04,NURSE ONLY,STKR

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828174244·102 P37,04,NURSE ONLY,STKR

    EPICARE-DUO LASER SYSTEM

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

    Persona Revision Knee System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CD 3700 SL

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·May 23, 2007

    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

    INVISION-PLUS

    FDA Adverse Event
    Malfunction ·RYMED TECHNOLOGIES, LLC·Product code FPA·July 7, 2022

    CELL-DYN 3700 SL ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·February 22, 2019

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·March 6, 2013

    ADAPTA DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code NVZ·August 8, 2014