BEUDAMED
    239 results · 20ms · Sources: EU EUDAMED, US FDA

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    FLH

    FDA Adverse Event
    Other ·STRYKER MEDICAL QUEBEC LP·Product code FNL·October 13, 2010

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·00801902094308·Arrowg+ard Blue(R) PSI Kit for use with 7.5 - 8...

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·00801902094322·ARROWg+ard Blue(R) Single-Lumen Central Venous ...

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·10801902120431·Arrowg+ard Blue(R) PSI Kit for use with 7 - 7.5...

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·00801902094339·ARROWg+ard Blue(R) Single-Lumen Central Venous ...

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·00801902094315·Arrowg+ard Blue(R) PSI Kit for use with 7 - 7.5...

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·10801902124330·ARROWg+ard Blue(R) Single-Lumen Central Venous ...

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·10801902120363·ARROWg+ard Blue(R) Single-Lumen Central Venous ...

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·10801902120462·Arrowg+ard Blue(R) PSI Kit for use with 7.5 - 8...

    ARROW

    FDA UDI
    TELEFLEX INCORPORATED·10801902146318·ARROW ENDURANCE(TM) Extended Dwell Peripheral C...

    METRIX AIR

    FDA Adverse Event
    Malfunction ·TRIVIDIA HEALTH, INC.·Product code NBW·June 26, 2017

    Arrow Endurance" Extended Dwell Peripheral Catheter System, REF: ASK-00820-FLH

    FDA Enforcement
    Class II ·Terminated·Arrow International Inc·January 29, 2020

    Arrow Endurance" Extended Dwell Peripheral Catheter System, REF: ASK-00820-FLH

    FDA Recall
    Terminated ·Arrow International Inc·Product code FOZ·December 6, 2019

    SP6000

    FDA Adverse Event
    Injury ·GETINGE DISINFECTION AB·Product code FLH·October 10, 2016

    120 CART WASHER

    FDA Adverse Event
    STERIS CANADA CORPORATION·Product code FLH·June 27, 2014

    RELIANCE 120 CART WASHER

    FDA Adverse Event
    STERIS CANADA CORPORATION·Product code FLH·June 26, 2014

    1227 CART WASHER

    FDA Adverse Event
    STERIS CANADA CORPORATION·Product code FLH·July 16, 2015

    TRANSPOSAL SAFETY STATION

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL, INC.·Product code FLH·November 8, 2017

    *

    FDA Adverse Event
    Malfunction ·DURO-MED INDUSTRIES·Product code FLH·December 28, 2012

    120 CART WASHER

    FDA Adverse Event
    STERIS CANADA CORPORATION·Product code FLH·October 3, 2014