BEUDAMED
    23 results · 22ms · Sources: EU EUDAMED, US FDA

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    XKNIFE 5

    FDA 510(k)
    FDA Class 2 ·Radiology

    Digital Analogue V3 SP

    FDA UDI
    RP - CONEXOES RESTAURADORAS LTDA·07901059074475·

    Bur PM2-70 50K Steel Ø0.8 St

    FDA UDI
    Bien-Air Surgery SA·17630055503739·

    Mirror™

    FDA UDI
    CAYENNE MEDICAL, INC.·M543100417·Two post femoral symmetric (Size 50mm)

    Label Printer Cable

    FDA UDI
    PATH medical GmbH·04260223140969·Label printer cable for Sentiero Desktop The La...

    GLOVER COOLEY BULLDOG CLAMP

    FDA UDI
    SONTEC INSTRUMENTS, INC.·B09921004170·GLOVER COOLEY BULLDOG CLAMP SPRING LOADED CURVED

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319702338·Spencer Stitch Scissors 4-3/8" (11cm), straight...

    Ortho Organizers

    FDA UDI
    Ortho Organizers, Inc.·00190707045999·.010 LIGATURE WIRE-1LB SPOOL

    CAL/RAD MARK IV-DOSE CALIBRATOR 34-162 VEENSTRA MODEL # VDC-304

    FDA 510(k)
    FDA Class 2 ·Radiology

    CONVERTORS EQUIPMENT DRAPES

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    GLIDEWIRE GT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·March 30, 2026

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·May 8, 2013

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 19, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 13, 2011

    ARCHITECT I2000SR ANALYZER

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·May 11, 2018

    GLIDEWIRE GT

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·May 29, 2026

    KING LAD Flexible ClearSeal SINGLE USE, King Systems ETO Sterilie, 10 devices/case "Size 4 / Adult ClearSeal Flexible King LAD¿ Patient Size: 50-70kg " Product Usage: Laryngeal airway

    FDA Enforcement
    Class II ·Terminated·King Systems Corp.·November 28, 2012

    RADIFOCUS GLIDEWIRE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·November 26, 2025

    CERELINK ICP PROBE BASIC KIT

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES SWITZERLAND SAR·Product code GWM·May 26, 2022

    TERUMO RADIFOCUS GUIDE WIRE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code DQX·July 3, 2025