BEUDAMED
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    BATTECH

    FDA registration
    BATTECH·47 products·🇺🇸 United States

    TOTALCARE-TREAT SURFACE&SCALE TOTAL CARE FRAME

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·December 4, 2009

    1 CC 29 GA INSULIN SYRINGE

    FDA Adverse Event
    Injury ·BECTON DICKINSON·Product code FMF·November 6, 2003

    CENTRA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·December 17, 2010

    BAXTER VIAFLEX TPN BAG

    FDA Adverse Event
    Malfunction ·*·Product code KPE·March 24, 2005

    HOMECHOICE AUTOMATED PD SET W/CASSETTE 4-PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FKX·March 14, 2002

    TOTALCARE-TREAT SURFACE&SCALE TOTAL CARE FRAME

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·August 11, 2009

    TOTALCARE-TREAT SURFACE&SCALE TOTAL CARE FRAME

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·August 20, 2009

    ASEPTIC BATTER HOUSING

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code KIJ·January 6, 2012

    VERSACARE BED VERSACARE FRAME

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·April 28, 2010

    BD INJECTOR N35-O¿

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·May 28, 2019

    BD PHASEAL¿ OPTIMA PROTECTOR (P20-O)

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·May 29, 2019

    CNS-6801A

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·April 4, 2021

    CNS-6801A

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·July 16, 2021

    MICRO DRILL MEDIUM STRAIGHT ATTECHMENT

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code ERL·November 7, 2011

    ZIMMER AIR DERMATOME

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL, INC.·Product code GFD·July 27, 2022

    CNS-6801A

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·July 16, 2021

    VASOVIEW HEMOPRO Endoscopic Vessel Harvesting System; Manufactured by Maquet Cardiovascular, LLC; 170 Baytech Drive, San Jose, CA 95134. Product Usage: Endoscopic vessel harvesting systems are indicated for use in minimally invasive surgery allowing access for vessel harvesting and are primarily indicated for patients undergoing endoscopic surgery for arterial bypass.

    FDA Recall
    Terminated ·Maquet Cardiovascular, LLC·Product code GEI·December 17, 2009

    VASOVIEW 7xB Endoscopic Vessel Harvesting System; Manufactured by Maquet Cardiovascular, LLC; 170 Baytech Drive, San Jose, CA 95134. Product Usage: Endoscopic vessel harvesting systems are indicated for use in minimally invasive surgery allowing access for vessel harvesting and are primarily indicated for patients undergoing endoscopic surgery for arterial bypass.

    FDA Recall
    Terminated ·Maquet Cardiovascular, LLC·Product code GEI·December 17, 2009

    VASOVIEW 6 Endoscopic Vessel Harvesting System Manufactured by Maquet Cardiovascular, LLC; 170 Baytech Drive, San Jose, CA 95134. Product Usage: Endoscopic vessel harvesting systems are indicated for use in minimally invasive surgery allowing access for vessel harvesting and are primarily indicated for patients undergoing endoscopic surgery for arterial bypass.

    FDA Recall
    Terminated ·Maquet Cardiovascular, LLC·Product code GEI·December 17, 2009