BEUDAMED
    101 results · 25ms · Sources: EU EUDAMED, US FDA

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    VAPR VUE RADIOFREQUENCY SYSTEM ,MODEL 225024, VPR VUE WIRELESS FOOTSWITCH, MODEL 227214

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

    Welch Allyn, Inc.

    FDA UDI
    WELCH ALLYN, INC.·00732094070767·CP 100 and CP 200 Connectivity Kit to the Cardi...

    WEITLANER RETRACTOR

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896049185·WEITLANER RETRACTOR HINGED BLUNT TIPS

    Leland Jones Clamp

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896103412·Leland Jones DeBakey Vascular Clamp

    Ortho Organizers

    FDA UDI
    Ortho Organizers, Inc.·00190707045074·16mm NITANIUM FORCE SPRING 300g

    APK

    FDA UDI
    APK Technology Co.,Ltd.·06946725547250·ECG Cable

    N/A

    FDA UDI
    Doppkon GmbH & Co. KG·04262494461798·Duck Jaw Punch Straight D 2.5mm, WL 330mm

    REMSTAR PLUS

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·January 29, 2025

    RESPONDER 3000

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    NEUROPLUS, MODEL A10040, A10041, A10042, A10043

    FDA 510(k)
    FDA Class 2 ·Neurology

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·April 28, 2025

    ENDURANT II

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code MIH·May 8, 2013

    NATURALYTE

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·September 17, 2014

    LEAD MODEL 302

    FDA Adverse Event
    Malfunction ·CYBERONICS INC.·Product code LYJ·May 12, 2011

    M2A-MAGNUM 52-60MM TAPER INSERT STD

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·May 18, 2012

    BI-METRIC/X POROUS COLLAR 13X145

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·May 18, 2012

    M2A-MAGNUM PF CUP 60ODX54ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·May 18, 2012

    M2A-MAGNUM MOD HEAD SZ54MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·May 18, 2012

    PROXIMATE*HCS HEMORR CIR STAPL

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 23, 2019

    Allura Xper FD10C; Model Number: 722001; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;

    FDA Recall
    Open, Classified ·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands·Product code OWB·September 3, 2025