BEUDAMED
    13 results · 30ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    H.R. JAKOBI SURG. INSTRUMENTS #11 13/20

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    PREGNA-CERT, SLIDE PREGNANCY TEST

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    REFEREE BRAND CO-OXIMETER REAGENTS

    FDA 510(k)
    FDA Class 2 ·Hematology

    BIOMET TIBIAL LOCKING BAR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·January 31, 2020

    VNGD PS OPEN POR FMRL RT 65

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 16, 2019

    E1 VNGD PS TIB BRG 71/75X10

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 16, 2019

    SERIES A PAT STD 31 3 PEG

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·October 16, 2019

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 27, 2014

    GYNECARE GYNEMESH* PS

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code FTL·November 15, 2012

    OCTRODE LEAD KIT, 60CM LENGTH

    FDA Adverse Event
    Injury ·ADVANCED NEUROMODULATION SYSTEMS·Product code LGW·September 13, 2010

    BIOMET FINNED PRI STEM 40MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBV·October 16, 2019

    TAPERLOC POR LAT FMRL 9X137

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·March 31, 2020

    M2A-MAGNUM 42-50 TPR INSRT STD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·November 4, 2019