BEUDAMED
    24 results · 27ms · Sources: EU EUDAMED, US FDA

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    Volo 14 Guidewire, 200cm, Soft Profile, Volo 14 Guidewire, 200cm, Standard Profile, Volo 14 Guidewire, 300cm, Soft Profile, Volo 14 Guidewire, 300cm, Standard Profile

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Integra® Miltex®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780362579·Integra® Miltex® Castroviejo Needle Holder, 5-1...

    ZOLL R SERIES BLS DEFIBRILLATOR

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    POWDER FREE LATEX EXAMINATION GLOVES (18 ML), BLUE TESTED FOR USE WITH CHEMOTHERAPY DRUGS

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ASTRON CLEAR SPLINTS

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code MQC·December 17, 2019

    GELB MOUTHGUARD

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code MQC·April 10, 2019

    ASTRON CLEAR SPRINT

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code MQC·January 14, 2020

    ASTRON CLEAR SPLINTS

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT INC.·Product code MQC·September 17, 2019

    ASTRON CLEAR SPLINTS

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code MQC·December 17, 2019

    ASTRON CLEAR SPLINTS

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code MQC·December 17, 2019

    ASTRON CLEAR SPLINTS

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT INC.·Product code MQC·September 16, 2019

    ASTRON CLEAR SPLINT

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code MQC·July 22, 2020

    ASTRON CLEAR SPLINT LOWER

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code MQC·January 30, 2020

    ASTRON CLEAR SPLINTS

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code MQC·May 4, 2020

    SHOULDER SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code PHX·July 28, 2025

    AESPIRE VIEW

    FDA Adverse Event
    Malfunction ·GE MEDICAL·Product code BSZ·October 10, 2014

    PAINSMART IOD

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·June 6, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 28, 2011

    ASTRON CLEAR SPLINTS

    FDA Adverse Event
    Injury ·PRISMATIK DENTALCRAFT, INC.·Product code MQC·July 2, 2020

    INSPIRA SMOOTH SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·April 17, 2025