BEUDAMED
    119 results · 24ms · Sources: EU EUDAMED, US FDA

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    SABER .035 PTA Dilatation Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AGXO

    FDA UDI
    Oticon A/S·05707131353542·G400 S, MINIRITE T 312 2.4G C090 AGXO

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613252634386·PED. MAND. DISTRACTOR, 3x3 RIGHT, 30 MM

    FAA Airline - 24 Metal

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588013237·FAA Airline - 24 Metal

    NAVIGATED INSTRUMENTS;PHOENIX SFS

    FDA UDI
    Orthofix US LLC·18257200121854·DILATOR SLEEVE, PHOENIX NAVIGATED

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523125555·Patella Trial Sz 4

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523125562·Patella Trial Sz 5

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523125524·Patella Trial Sz 1

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523125531·Patella Trial Sz 2

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523125548·Patella Trial Sz 3

    ARTEMIS

    FDA 510(k)
    FDA Class 2 ·Radiology

    AGILENT COMPONENT MONITORING SYSTEM, AGILENT MULTI-MEASUREMENT SERVER AND COMPACT PORTABLE PATIENT MONITOR, AGILENT NONI

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    TENSION FREE VAGINAL TAPE - OBTURATOR UNKNOWN PROD

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·November 6, 2018

    HEARTSTREAM FR2

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 26, 2013

    RESTORE ULTRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·August 3, 2011

    COULTER LH 750 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·October 27, 2014

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·September 18, 2015

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC·Product code GJS·October 25, 2013

    ARCHITECT CA 19-9XR

    FDA Adverse Event
    Malfunction ·ABBOTT LABORATORIES·Product code NIG·September 19, 2013

    ONYX LES

    FDA Adverse Event
    Injury ·COVIDIEN (IRVINE)·Product code MFE·April 24, 2017