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

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    ORTHOVITA PEEK SPACER

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Alpen Carbides

    FDA UDI
    Dent4You AG·07630392906029·Alpen Carbides 1171-FG-1.20-4.10, 10 pcs

    Tasso+ Convenience Kit

    FDA UDI
    Tasso Inc.·00860006434526·Tasso+ allows self-collection of a capillary bl...

    OrthoMedFlex

    FDA UDI
    ORTHOMEDFLEX LLC·M7161011710·Straight Cup Impactor

    NA

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295000532·PROTRUSIO CAGE CEMENTED ACETABULAR RECONSTRUCTI...

    TAMPAX SCENTED & SATIN SCENTED TAMPAX-JUNIOR, REGULAR, SUPER & SUPER PLUS

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    DELTA 16 TACT

    FDA 510(k)
    FDA Class 2 ·Radiology

    V-GO DISPOSABLE INSULIN DELIVERY DEVICE

    FDA Adverse Event
    Injury ·ZEALAND PHARMA U.S. INC.·Product code LZG·June 28, 2021

    POWERLINK SYSTEM

    FDA Adverse Event
    Injury ·ENDOLOGIX, INC·Product code MIH·October 21, 2010

    UNKNOWN BEARING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·April 20, 2026

    UNK BEARING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·April 2, 2026

    UNK GLENOSPHERE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·April 2, 2026

    ELLIPSE DR, DF4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 9, 2013

    GRANUFLO

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·September 3, 2014

    INSTRUMENT ADAPTER, STARLOCK INTERFACE

    FDA Adverse Event
    Other ·BRAINLAB AG·Product code HAW·May 17, 2011

    SYRINGE S2 20ML 18GA 1-1/2IN BD CHINA

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·July 28, 2021

    TRIAL STEM for MP(R) RECONSTRUCTION PROTHESIS, REF 99-0155/20, Stem size S-4, prox. Stem dia. 20 mm, Length 180 mm, WALDEMAR LINK GmbH & CoKG, Barkhausenweg 10 . D . 22339 Hamburg

    FDA Enforcement
    Class II ·Terminated·Waldemar Link GmbH & Co. KG (Corp. Hq.)·September 4, 2013

    BATTERY RECIPROCATOR II FOR BPL II

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES PRODUCTS LLC·Product code GEY·May 7, 2020

    UNK TM BASEPLATE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·April 15, 2026

    UNK TM BEARING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·April 15, 2026