BEUDAMED
    10,000 results · 49ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    Lapidus Plate, Beta

    FDA UDI
    FLOWER ORTHOPEDICS CORPORATION·00840118111898·implants for orthopedic bone fixation

    Elongated L-Plate, 5 Holes, (L),

    FDA UDI
    FLOWER ORTHOPEDICS CORPORATION·00840118104999·Compatible with 2.7mm/3.0mm screws, implants fo...

    1.7mm Elongated L-Plate, 5 Holes, (R),

    FDA UDI
    FLOWER ORTHOPEDICS CORPORATION·00840118104982·Compatible with 2.7mm/3.0mm screws, implants fo...

    Lapidus Plate, Alpha

    FDA UDI
    FLOWER ORTHOPEDICS CORPORATION·00840118111881·implants for orthopedic bone fixation

    Elongated L-Plate, 4 Holes, (L)

    FDA UDI
    FLOWER ORTHOPEDICS CORPORATION·00840118104975·Compatible with 2.7mm/3.0mm screws, implants fo...

    Elongated L-Plate, 4 Holes, (R),

    FDA UDI
    FLOWER ORTHOPEDICS CORPORATION·00840118104968·Compatible with 2.7mm/3.0mm screws, implants fo...

    THE LF-P CERAMIC SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    TRACHEAL INTUBATION FIBERSCOPE

    FDA UDI
    OLYMPUS MEDICAL SYSTEMS CORP.·04953170051098·LF-P INTUBATION FIBERSCOPE

    TRACHEAL INTUBATION FIBERSCOPE

    FDA UDI
    OLYMPUS MEDICAL SYSTEMS CORP.·04953170452932·

    IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·September 13, 2021

    INS 37604 ACTIVA PC+S NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code MHY·January 26, 2017

    PERCEPT

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code MHY·November 16, 2021

    SPRINT QUATTRO SECURE S

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 14, 2012

    UNKNOWN IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·June 12, 2015

    Tracheal Intubation Fiberscope OLYMPUS LF-P, VISERA Tracheal Intubation Videoscope OLYMPUS LF Type V

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

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code MHY·October 31, 2016

    SPRINT QUATTRO

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·February 16, 2012

    PROTECTA CRT-D

    FDA Adverse Event
    Malfunction ·MEDTRONIC S.A.·Product code NIK·February 16, 2012

    IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MRU·June 29, 2021

    IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·June 29, 2021