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

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    Collagen Dural Regeneration Matrix

    FDA 510(k)
    FDA Class 2 ·Neurology

    HHM

    FDA UDI
    Oticon A/S·05707131281678·H150V2, BTE 13 WL 100 SIL HHM

    Globe Scientific

    FDA UDI
    GLOBE SCIENTIFIC INC.·00840095620147·Filter tip, 1-200uL XL/300uL, 59mm,low retentio...

    BIOMET KNEE SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304007277·

    Bioseal Inc.

    FDA UDI
    BIOSEAL·00630094015088·Impervious Stockinette 6"x30" CSR Wrapped

    Biomet® Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00887868344312·

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197541909·RZ Tebbet Breast Retractor 150x25...

    PHILIPS HEARTSTART XL+, PHILIPS HEARTSTART EXTERNAL PADDLES, PHILIPS MULTIFUNCTION ELECTRODES

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    SUPRA SCAN DELIVERY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    BD MULTI-CHECK CD4 LOW CONTROL

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·August 29, 2023

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·June 6, 2013

    STYLE 163 SALINE FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN·Product code FWM·June 2, 2011

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 8, 2014

    DIVA

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 7, 2020

    DIVA

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·July 7, 2020

    PRODIGY VOICE

    FDA Adverse Event
    Injury ·OK BIOTECH CO., LTD.·Product code NBW·July 8, 2016

    SENRI

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code DQY·December 25, 2016

    BD MULTI-CHECK CD4 LOW CONTROL

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·August 16, 2023

    PRODIGY AUTOCODE

    FDA Adverse Event
    Injury ·OK BIOTECH CO., LTD.·Product code NBW·December 27, 2016

    METACROSS RX PTA BALLOON DILATATION CATHETER

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·October 15, 2019