BEUDAMED
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    POST SURGICAL MFG.

    FDA registration
    POST SURGICAL MFG.·12 products·🇺🇸 United States

    LIGACLIP ENDOSCOPIC SINGLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·POST SURGICAL MFG·Product code GDO·July 2, 1998

    LIGACLIP ENDOSCOPIC SINGLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·POST SURGICAL MFG·Product code GDO·July 2, 1998

    LIGACLIP ENDOSCOPIC SINGLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·POST SURGICAL MFG·Product code GDO·February 7, 2000

    LIGACLIP SINGLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·POST SURGICAL MFG·Product code FZP·March 9, 2001

    LIGACLIP SINGLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·POST SURGICAL MFG·Product code FZP·April 20, 2001

    LIGACLIP ENDOSCOPIC SINGLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·POST SURGICAL MFG.·Product code GDO·December 15, 1998

    LIGACLIP ENDOSCOPIC SINGLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·POST SURGICAL MFG·Product code GDO·December 17, 1998

    LIGACLIP ENDOSCOPIC SINGLE CLIP APPLIER

    FDA Adverse Event
    Malfunction ·POST SURGICAL MFG.·Product code GDO·December 15, 1998

    HARMONIC SCALPEL COAGULATING SHEARS WITH SCISSORGRIP

    FDA Adverse Event
    Malfunction ·POST SURGICAL MFG, INC.·Product code LFL·October 20, 1998

    COONRAD/MORREY PIN/BUSHING REPLACEMENT KIT

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JDC·February 15, 2011

    50CM IMPLANT LEAD KIT, SLIM TIP

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code PMP·March 20, 2019

    50CM IMPLANT LEAD KIT, SLIM TIP

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code PMP·March 20, 2019

    EXCLAIM LEAD, 90 CM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·April 24, 2019

    CANCELLO-PURE WEDGE

    FDA Adverse Event
    Injury ·RTI BIOLOGICS·Product code MQV·June 13, 2012

    50CM IMPLANT LEAD KIT, SLIM TIP

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code PMP·May 8, 2019

    50CM IMPLANT LEAD KIT, SLIM TIP

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code PMP·May 8, 2019

    PROCLAIM 5 ELITE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, LLC)·Product code LGW·April 24, 2019

    GORE EXCLUDER BIFURCATED ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·April 12, 2006

    ZIMMER PERIARTICULAR LOCKING TIBIAL PLATE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code HRS·September 16, 2010