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

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    DIAPHYSEAL PLATE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    REMEL

    FDA UDI
    REMEL, INC.·00848838006067·Bile Esculin Agar (slant) 20/PK

    Mini Mono®

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR70602941·Mini-Mono-Brackets 4th Dim. Ricketts 'S' .018" ...

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306813474·Russian Tissue Forceps, 25cm

    MFCD 120

    FDA 510(k)
    FDA Class 2 ·Radiology

    MOTION TRACKING

    FDA 510(k)
    FDA Class 2 ·Radiology

    HEARTSTREAM FR2

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·April 11, 2013

    54 CM STEROID ELUTING BIPOLAR LEAD

    FDA Adverse Event
    Malfunction ·GREATBATCH MEDICAL·Product code DTB·August 8, 2014

    SELECTSITE DEFLECTABLE CATH

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code DQY·April 15, 2011

    TESS HUM INSERT TH 6 DIA36 S1

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code KWS·March 7, 2017

    TESS HUMERAL INSERT TH 8 DIA36 S0

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code KWS·February 15, 2017

    NMIC-312

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 16, 2026

    PANEL PHOENIX NMIC-312

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 3, 2026

    TESS HUMERAL REVERSED INLAY 036 S1 12MM

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·February 9, 2017

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 15, 2026

    TESS HUMERAL INSERT TH 6 DIA36 S0

    FDA Adverse Event
    Malfunction ·BIOMET FRANCE S.A.R.L.·Product code KWS·February 15, 2017

    CUSTOM REVERSE HUMERAL LINER

    FDA Adverse Event
    Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·February 27, 2017

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 8, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026

    BD PHOENIX¿ NMIC/ID-307

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON & CO. (SPARKS)·Product code LON·May 5, 2026