BEUDAMED
    14 results · 20ms · Sources: EU EUDAMED, US FDA

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    METIC™- Airway Balloon Catheter

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    MILAGRO

    FDA UDI
    Medos International Sàrl·10886705022342·Milagro Advance Interference Screw Absorbable-T...

    CASTANEDA ENUCLEATION FORCEPS

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896019843·CASTANEDA ENUCLEATION FORCEPS ATRAUMATIC CURVED...

    VITAL SIGNS MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FACILAI VARIOUS MODELS OF SINGLE USE ACUPUNCTURE NEEDLE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TEXIUM

    FDA Adverse Event
    Malfunction ·SISTEMAS MEDICOS ALARIS S.A DE C.V.·Product code FMF·March 19, 2026

    REDUCTION BALL END DRIVER

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK INSTRUMENT MANUFACTURING·Product code HXX·September 1, 2011

    PIPELINE EMBOLIZATION DEVICE

    FDA Adverse Event
    Malfunction ·EV3 NEUROVASCULAR·Product code OUT·December 6, 2012

    TRADITION PUSH BUTTON FIBER OPTIC HS HANDPIECE

    FDA Adverse Event
    Malfunction ·DENTSPLY PROFESSIONAL·Product code EFB·October 15, 2014

    MILAGRO ADVANCE SCREW 9X23MM

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·February 27, 2019

    9X23MM MILAGRO ADVANCE INTERFERENCE SCREW

    FDA Adverse Event
    Injury ·DEPUY MITEK·Product code MAI·September 12, 2017

    MILAGRO ADVANCE SCREW 9X23MM

    FDA Adverse Event
    Malfunction ·DEPUY MITEK LLC US·Product code MAI·October 6, 2023

    INTRAFIX TAPERED SCREW 6-8MM X 30MM (ACETAL/DELRIN)

    FDA Adverse Event
    Injury ·DEPUY MITEK·Product code MBI·July 21, 2014

    Revogene, Catalog no. 610210. IVD test instrument

    FDA Enforcement
    Class II ·Ongoing·Meridian Bioscience Inc·August 3, 2022