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

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    FDA 510(k)
    FDA Class 2 ·Radiology

    Oticon

    FDA UDI
    Oticon A/S·05707131340832·G40 FW 6.0

    Pre-Finisher

    FDA UDI
    TP ORTHODONTICS INC·00192029041512·Non-Extraction

    REUSABLE LINEAR STAPLER HANDLE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ATLAS IMPLANT SYSTEM- MINI PLUS

    FDA 510(k)
    FDA Class 2 ·Dental

    COMPOSIX MESH E/X

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·October 3, 2008

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 18, 2013

    5.5MM BIOCOMPOSITE CORK- SCREW FT W2#2 TIGERTAIL

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code MAI·August 4, 2011

    GALAXY G3 MINI 2MM X 4CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·June 16, 2021

    GALAXY G3 5MM X 15CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·June 16, 2021

    GALAXY G3 MINI 3MM X 8CM

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·June 16, 2021