BEUDAMED
    7,144 results · 29ms · Sources: EU EUDAMED, US FDA

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    MVS-MODEL SEU-6, DEU-6

    FDA 510(k)
    FDA Class 1 ·Dental

    DreamStation Travel Kit, 65W P/S, EU

    Device
    EU MDD · Eu Md Class 2a ·Respironics Inc.·On the market·26 countries

    Epicage

    FDA UDI
    ALPHATEC SPINE, INC.·00844856062832·EPICAGE - PEEK MEDIUM SPACER - 30MM X 10MM - ST...

    Epicage

    FDA UDI
    ALPHATEC SPINE, INC.·00844856062771·EPICAGE - PEEK MEDIUM SPACER - 25MM X 12MM - ST...

    Epicage

    FDA UDI
    ALPHATEC SPINE, INC.·00844856062856·EPICAGE - PEEK MEDIUM SPACER - 30MM X 12MM - ST...

    Globe Scientific

    FDA UDI
    GLOBE SCIENTIFIC INC.·00840095608404·Centrifuge, Clinical, 12-Place, 240v, 50Hz, EU ...

    Epicage

    FDA UDI
    ALPHATEC SPINE, INC.·00844856062733·EPICAGE - PEEK MEDIUM SPACER - 25MM X 8MM - STE...

    Epicage

    FDA UDI
    ALPHATEC SPINE, INC.·00844856062757·EPICAGE - PEEK MEDIUM SPACER - 25MM X 10MM - ST...

    Epicage

    FDA UDI
    ALPHATEC SPINE, INC.·00844856062795·EPICAGE - PEEK MEDIUM SPACER - 25MM X 14MM - ST...

    Epicage

    FDA UDI
    ALPHATEC SPINE, INC.·00844856062870·EPICAGE - PEEK MEDIUM SPACER - 30MM X 14MM - ST...

    Epicage

    FDA UDI
    ALPHATEC SPINE, INC.·00844856062818·EPICAGE - PEEK MEDIUM SPACER - 30MM X 8MM - STE...

    MVS UNIT, MODEL SEU-8 AND DEU-8, 80

    FDA 510(k)
    FDA Class 1 ·Dental

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810057373794·E-Z Lift Beach Chair with Connection Holder (EU)

    SYSMEX PS-10

    FDA Adverse Event
    Malfunction ·SYSMEX CORPORATION·Product code PER·January 9, 2025

    REPLY 200

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA S.R.L. - CRM FACILITY·Product code DTB·August 31, 2015

    ALPHATEC SOLUS LUMBER SPACER, STERILE (TI-6AL

    FDA Adverse Event
    Malfunction ·ALPHATEC SPINE INC·Product code OVD·January 15, 2015

    S-ICD SYSTEM

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 30, 2018

    EMBLEM MRI S-ICD

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LWS·June 24, 2022

    REPLY

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA S.R.L. - CRM FACILITY·Product code DXY·May 5, 2017

    OB SUPER 48 S EU

    FDA Adverse Event
    Injury ·NI·Product code HEB·September 13, 2012