BEUDAMED
    15 results · 31ms · Sources: EU EUDAMED, US FDA

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    Synergy Cranial

    FDA 510(k)
    FDA Class 2 ·Neurology

    DIVERGENCE-L™ Anterior/Oblique Lumbar Fusion System

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00643169524804·GUIDE 2150216 O51 SCREW GUIDE 16MM

    HHM

    FDA UDI
    Oticon A/S·05707131286413·H160V2 TI, MINIRITE 312 WL DBL HHM

    Accent Buccal Tube

    FDA UDI
    ORMCO CORPORATION·00889989054064·ORTHOS ACCENT USM 15SGL WDX -10TX18 L

    RZ Medizintechnik GmbH

    FDA UDI
    RZ-Medizintechnik GmbH·04049197511247·Tebbet Breast Retractor 150x16...

    EXPEDIUM SYSTEM, VIPER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OMNILUX REVIVE AND OMNILUX PLUS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    OT VERIO FLEX METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 1, 2015

    PAINSMART IOD

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·May 29, 2013

    GOBED II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·June 10, 2011

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM

    FDA Adverse Event
    Injury ·BIOENTERICS CORP.·Product code LTI·September 3, 2008

    BIPOLAR INSERT, MODULAR¸ 42/28

    FDA Adverse Event
    Injury ·ZIMMER SWITZERLAND MANUFACTURING GMBH·Product code LPH·June 20, 2023

    HERMETIC LUMBAR CATHETER, CLOSED TIP

    FDA Adverse Event
    Malfunction ·INTEGRA NEUROSCIENCES PR·Product code JXG·September 26, 2016

    MEDTRONIC DUAL CHAMBER TEMPORARY EXTERNAL PACEMAKER 510(K) K150246

    FDA Adverse Event
    Death ·MEDTRONIC, INC.·Product code DTE·February 10, 2021

    TREVO XP PROVUE 4MM X 30MM

    FDA Adverse Event
    Injury ·STRYKER NEUROVASCULAR-UTAH-SALT LAKE CITY·Product code NRY·July 24, 2020