BEUDAMED
    22 results · 35ms · Sources: EU EUDAMED, US FDA

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    KATALYST LASER PROBES, KATALYST ILLUMINATED LASER PROBES

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776392635·Debakey TC Needle Holder, delicate, serrated, 9"

    Integra® Jarit®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780377382·Integra® Jarit® DeBakey Vascular Needle Holder,...

    CHS

    FDA UDI
    Smith & Nephew, Inc.·03596010062598·COMPRESSION HIP SCREW SUPER LAG SCREW 90MM

    PATCH, PLEDGET AND INTRACARDIAC

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FM-1000 PLUS FETAL MONITOR

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    FASTTAKE

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·July 22, 2002

    ONE TOUCH ULTRA

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·August 9, 2002

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 21, 2024

    MECHANICAL CHAIR/TRANSPORT CHAIR

    FDA Adverse Event
    DANYANG HUAYI MEDICAL SUPPLY&EQUIPMENT CO.,LTD·Product code INM·May 20, 2013

    CONSOLE 110V(PEDAL&POLE INCLD)

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-INAGI·Product code LFL·September 26, 2014

    UNKNOWN DEPUY ASR CUP

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD.·Product code KWA·June 1, 2011

    TECNIS IOL

    FDA Adverse Event
    Malfunction ·AMO PUERTO RICO MFG. INC.·Product code MJP·March 15, 2024

    TECNIS IOL

    FDA Adverse Event
    Malfunction ·AMO PUERTO RICO MFG. INC.·Product code MJP·March 15, 2024

    TECNIS IOL

    FDA Adverse Event
    Malfunction ·AMO PUERTO RICO MFG. INC.·Product code MJP·March 15, 2024

    TECNIS IOL

    FDA Adverse Event
    Malfunction ·AMO PUERTO RICO MFG. INC.·Product code MJP·March 15, 2024

    ARROW CVC SET: 16 GA X 8" (20 CM)

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code DQY·September 5, 2017

    Siemens Artis Q biplane---Interventional Fluoroscopic X-Ray System Model Number: 10848282

    FDA Enforcement
    Class II ·Terminated·Siemens Medical Solutions USA, Inc·July 10, 2019

    Artis Q biplane, Model Number 10848282

    FDA Enforcement
    Class II ·Ongoing·Siemens Medical Solutions USA, Inc·April 27, 2022

    Artis Q Interventional Fluoroscopic X-Ray System, Model Numbers 10848280, 10848281, 10848282, 10848283, 10848354 & 10848355

    FDA Enforcement
    Class II ·Terminated·Siemens Medical Solutions USA, Inc·September 26, 2018