BEUDAMED
    56 results · 37ms · Sources: EU EUDAMED, US FDA

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    RESOLUTION CLIP MODEL M00522600, M00522601, M00522602, M00522610, M00522611, M00522612

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PIVOX™ Oblique Lateral Spinal System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169606517·SPACER 2122660 O25 23.5MM 12 DEG 18X60

    ArgenZ HT+ 95x10 A3.5

    FDA UDI
    ARGEN CORPORATION, THE·D818122660·Dental porcelain/ceramic restoration kit

    RUSCH

    FDA UDI
    TELEFLEX INCORPORATED·14026704624512·RUSCH Color Coded Guedel Airway Length 60mm Tra...

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16741226600·

    SINGER CAPSULE SWEEP ANTERIOR POLSHER

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896013315·SINGER CAPSULE SWEEP ANTERIOR POLSHER DOUBLE EN...

    SINGER CAPSULE SWEEP ANTERIOR POLSHER

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896013308·SINGER CAPSULE SWEEP ANTERIOR POLISHER DOUBLE E...

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1674122660060·

    BIOCHECK MYOGLOBIN ELISA, MODEL BC-1117

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    BIORAPTOR CURVED 2.3 PK SUTURE ANCHORS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AXOGUARD NERVE CONNECTOR AND PROTECTOR

    FDA Adverse Event
    Injury ·COOK BIOTECH·Product code JXI·August 24, 2015

    LIFEPAK(R) 1000 DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·July 10, 2015

    PROFEMUR(R) MODULAR FEMORAL NECK

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LWJ·May 21, 2013

    POWERED WHEELCHAIR

    FDA Adverse Event
    Malfunction ·INVACARE TAYLOR STREET·Product code ITI·September 26, 2014

    PFC SIGMA/OV/DOME PAT 3PEG, 41

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·June 3, 2011

    LIFEPAK® 1000 DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC. - 3015876·Product code MKJ·April 24, 2019

    CMK OC - RASP S303

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code LZO·January 28, 2026

    CMK OC - RASP S303

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code LZO·January 28, 2026

    CMK OC - RASP S202

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code LZO·February 5, 2026

    CMK OC - RASP S302

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code LZO·February 5, 2026