BEUDAMED
    43 results · 23ms · Sources: EU EUDAMED, US FDA

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    Monocryl Plus Antibacterial Suture

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

    BOLTON PTA CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEPUY GLOBAL UNITE SHOULDER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    *

    FDA Adverse Event
    Malfunction ·MCGHAN MEDICAL CORP.·Product code FWM·April 1, 1998

    STERNGOLD IMPLAMED, FIXTURE, TI,

    FDA Adverse Event
    Injury ·STERNGOLD IMPLAMED·Product code DZE·February 16, 1998

    STERNGOLD IMPLAMED, FIXTURE, TI,

    FDA Adverse Event
    Injury ·STERNGOLD IMPLAMED·Product code DZE·February 16, 1998

    DEPUY ACE 4.5MM CORTICAL BONE SCREW

    FDA Adverse Event
    Malfunction ·DEPUY ACE MEDICAL COMPANY·Product code HWC·August 14, 1997

    APR HOODED ENHANCED INSERT 28MM/59MM

    FDA Adverse Event
    Injury ·SULZER ORTHOPEDICS, INC.·Product code KWB·July 24, 1997

    NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM FOR ADULTS

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·January 31, 1997

    QUINTON TENCKHOFF PERITONEAL CATHETER

    FDA Adverse Event
    Injury ·QUINTON INSTRUMENT CO.·Product code FJS·December 21, 1998

    ITREL 3

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code GZB·October 30, 1998

    MEDI-JECTOR

    FDA Adverse Event
    Injury ·MEDI-JECT CORP.·Product code KZE·August 7, 1996

    MERSILENE POLYESTER FIBER MESH

    FDA Adverse Event
    Injury ·ETHICON, INC. SAN LORENZO·Product code FTL·April 14, 2000

    NEXGEN IM FEMORAL A/P SIZING GUIDE

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code FZX·February 14, 2013

    INSPIRE OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·March 4, 2026

    VERIFLEX

    FDA Adverse Event
    Malfunction ·NUCLETRON CORP·Product code IWB·October 15, 1996

    840 VENTILATOR

    FDA Adverse Event
    Malfunction ·COVIDIEN, FORMELRY NELLCO·Product code CBK·June 27, 2013

    CONCERTO CRT-D DR

    FDA Adverse Event
    Injury ·MEDTRONIC MED REL, INC.·Product code NIK·August 11, 2011

    RESOLUTION

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP.·Product code MND·August 28, 2014

    INSPIRE OXYGENATOR

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·November 20, 2025