BEUDAMED
    12 results · 20ms · Sources: EU EUDAMED, US FDA

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    CORDIS WEBSTER PREFACE BRAIDED GUIDING SHEATH & PERRY EXCHANGE DILATOR, MODEL #'S 301-803A, 301-803P, 301-803M, 301-813S

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Invictus

    FDA UDI
    ALPHATEC SPINE, INC.·00190376301761·In-Situ Coronal Bender Tip, Right, 4.0mm

    GC AADVA ZR DISK

    FDA 510(k)
    FDA Class 2 ·Dental

    ACCESS R-CLONE(TM) ANA/RF SCREENING ASSAY

    FDA 510(k)
    FDA Class 2 ·Immunology

    CER OPTION TYPE 1 TPR SLEVE +6

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LZO·July 31, 2019

    RADIESSE FILLER

    FDA Adverse Event
    Injury ·MERZ AESTHETICS·Product code LMH·February 24, 2013

    ARCOS TORQUE LIMITING T-HANDLE 55IN.-LBS.

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS·Product code MDM·February 9, 2011

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 24, 2014

    G7 PPS LTD ACET SHELL 60G

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PBI·July 31, 2019

    TPRLC 133 T1 PPS HO 13X146MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·July 31, 2019

    G7 NEUTRAL E1 LINER 40MM G

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PBI·July 31, 2019

    CER OPTION TYPE 1 TPR SLEVE +6

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·October 8, 2019