BEUDAMED
    19 results · 21ms · 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.

    LOMBARD DOWELL AGAR BASE

    FDA 510(k)
    FDA Class 1 ·Microbiology

    NTI

    FDA UDI
    NTI - Kahla GmbH Rotary Dental Instruments·E310864014CFG1·NTI Diamond Coarse FG

    NTI

    FDA UDI
    NTI - Kahla GmbH Rotary Dental Instruments·E310864014FFG1·NTI Diamond Fine FG

    Trabecular Metal®

    FDA UDI
    Zimmer, Inc.·00889024139275·

    Trabecular Metal®

    FDA UDI
    Zimmer, Inc.·00889024139282·

    BUSCH®, BNA®

    FDA UDI
    BUSCH & CO. GmbH & Co. KG·D8120354301·Diamond, flame, fine grit, red ring

    BUSCH®, BNA®

    FDA UDI
    BUSCH & CO. GmbH & Co. KG·D8120307271·Diamond, flame, medium grit

    ONO/CO-TWO (TM) SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Microbiology

    POTATO DEXTROSE AGAR

    FDA 510(k)
    FDA Class 1 ·Microbiology

    DUROM US ACETABULAR COMPONENT 52/46 L

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·March 5, 2019

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·June 10, 2014

    CONTAK RENEWAL

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·October 11, 2010

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·December 10, 2012

    METASUL LDH, HEAD, 48, CODE N, TAPER 18/20

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code KWA·August 11, 2021

    DUROM US ACET CMPNT 54/48 N

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code KWA·August 11, 2021

    Zimmer Trabecular metal primary hip prosthesis femoral stem, press-fit, collarless, 12/14 neck taper - standard body -extended neck offset, size 14, 149 mm stem length, sterile, tivanium TI-6AL-4V alloy/tantalum, sterile; Cat. no. 00-7864-014-20 (00786401420).

    FDA Recall
    Terminated ·Zimmer Inc.·Product code LPH·August 2, 2006

    METASUL® LDH®, HEAD ADAPTER, XL, +8, TAPER 12/14-18/20

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code KWA·April 13, 2022

    DUROM US ACET CMPNT 54/48 N

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code KWA·April 13, 2022

    METASUL® LDH®, HEAD, 48, CODE N, TAPER 18/20

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code KWA·April 13, 2022