BEUDAMED
    21 results · 23ms · Sources: EU EUDAMED, US FDA

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    ATTIVA

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

    SMARTLOCK

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·34546540365324·Locking Screws, Cross-Pin

    ELMED

    FDA UDI
    ELMED INCORPORATED·00842180164017·5 MM DIA., PYRAMIDAL TROCAR FOR 150MM WORKING L...

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613327090468·FRACTURE PLATE, WITH BAR

    Zavation

    FDA UDI
    Zavation LLC·00842166132733·Ti3Z CIF 14mmx16mmx5mm -5 deg

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707022329·CALIBRA BANDS 2ND MOLAR n.SUR 5

    SYNTHES TRANSLATING MAXILLARY DISTRACTOR

    FDA 510(k)
    FDA Class 2 ·Dental

    FRESENIUS 2008T HEMODIALYSIS MACHINE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    BD VACUTAINER® BUFFERED SODIUM CITRATE (9NC) BLOOD COLLECTION TUBE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·January 28, 2020

    CANCELLOUS SCREW, Ø6.5MM X 85MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HSB·March 7, 2024

    ANTEGRADE FEM NAIL, LEFT, Ø10MM X 40CM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HSB·March 7, 2024

    CAPTURED CORTICAL SCREW, Ø5.0MM X 50MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HSB·March 7, 2024

    SCHILLER

    FDA Adverse Event
    Malfunction ·LEONHARD LANG GMBH·Product code MKJ·May 30, 2023

    CAPTURED CORTICAL SCREW, Ø5.0MM X 55MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HSB·March 7, 2024

    CANCELLOUS SCREW, Ø6.5MM X 85MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HSB·March 7, 2024

    CANCELLOUS SCREW, Ø6.5MM X 90MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HSB·March 7, 2024

    DERMAGRAFT

    FDA Adverse Event
    Other ·ADVANCED BIOHEALING, INC·Product code MGR·October 16, 2008

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·July 18, 2011

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 11, 2013

    Abbott Alinity m System, REF 08N53-002, containing Amplification Detetction Unit (ADU) #4.

    FDA Enforcement
    Class II ·Ongoing·Abbott Molecular, Inc.·April 12, 2023