BEUDAMED
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    FDA UDI
    TELEFLEX INCORPORATED·10801902112313·Pressure Injectable ARROWg+ard Blue PLUS(R) Two...

    UNK - CONSTRUCTS: PHILOS PLATE/SCREWS

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HRS·July 27, 2022

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·April 24, 2026

    CONSERVE(R) PLUS BFH TOTAL HIP

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KWA·May 16, 2013

    UNKNOWN COMPREHENSIVE REVERSE GLENOSPHERE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·September 10, 2025

    UNKNOWN COMPREHENSIVE REVERSE TRAY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·September 10, 2025

    UNKOWN COMPREHENSIVE REVERSE BEARING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·September 10, 2025

    UNKNOWN COMPREHENSIVE REVERSE STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·September 10, 2025

    UNKNOWN COMPREHENSIVE REVERSE TRAY

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·September 10, 2025

    UNKNOWN COMPREHENSIVE REVERSE BASEPLATE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·September 10, 2025

    UNKNOWN COMPREHENSIVE REVERSE BASEPLATE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·September 10, 2025

    SCREW,FIXATION,BONE

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·January 30, 2019

    PLATE,FIXATION,BONE

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·January 30, 2019

    ECHELON ENDOPATH STAPLER

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·July 1, 2025

    TORNIER PERFORM REVERSED LATER ALIZED BASEPLATE 3MM DIA 25MM

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code PHX·June 26, 2023

    PLATE,FIXATION,BONE

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·January 30, 2019

    SCREW,FIXATION,BONE

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·January 30, 2019

    SCREW,FIXATION,BONE

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·January 30, 2019

    PLATE,FIXATION,BONE

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HRS·January 30, 2019

    Arrowgard Blue and Arrowgard Blue Plus Pressure Injectable Central Venous Catheter, a multiple-lumen catheter that permits venous access to central circulation. Catalog number ASK-45703-PHF.

    FDA Recall
    Terminated ·Arrow International Inc·Product code FOZ·July 17, 2013