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

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    FDA 510(k)
    FDA Class 2 ·Radiology

    ARKEO, Wedge Fixation System

    FDA UDI
    Auxano Medical LLC·00850055649927·ARKEO Evan's Wedge Trial, 20x20x08

    SANTORINI™ Corpectomy Cage System

    FDA UDI
    VB Spine LLC·10888857021129·Solid Cage

    Introcan Safety ® 2

    FDA UDI
    B. BRAUN MEDICAL INC.·04046955746026·Introcan Safety® 2 IV Catheter - 20 Ga. x 1.25 in.

    ULTRAVISUAL

    FDA 510(k)
    FDA Class 2 ·Radiology

    MYLABSEVEN, MYLABALPHA

    FDA 510(k)
    FDA Class 2 ·Radiology

    ONCENTRA MASTERPLAN

    FDA Adverse Event
    Malfunction ·NUCLETRON B.V.·Product code MUJ·July 14, 2008

    ONCENTRA MASTERPLAN

    FDA Adverse Event
    Malfunction ·NUCLETRON B.V.·Product code MUJ·July 14, 2008

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON RESEARCH LTD / HUNTINGTON·Product code HQL·April 24, 2008

    ENDOPATH DEXTRUS SEAL CAP ASSEMBLY WITH ACCESSORIES

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC·Product code GCJ·February 20, 2009

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·November 10, 2014

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 9, 2011

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2013

    PROX ACCESS 55MM ART STAP REG

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC. (CINCINNATI)·Product code GDW·February 20, 2009

    CARPENTIER-EDWARDS PERIMOUNT PLUS PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code LWR·October 29, 2008

    PROXIMATE PPH PROCEDURE SET

    FDA Adverse Event
    Injury ·ETHICON ENDO SURGERY, INC (CINCINNATI)·Product code GDW·April 25, 2008

    JEHLE CATH 4-HEAD STERILE 5/BX

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code DYB·April 8, 2008

    LIGAMAX-5MM ENDO CLIP APPLIER

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code FZP·February 20, 2009

    LAP DISC HAND ACCESS DRIVE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCIANNTI)·Product code GCJ·June 24, 2008

    HARMONIC ACE 36 CM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·September 24, 2008