BEUDAMED
    20 results · 70ms · Sources: EU EUDAMED, US FDA

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    WALLACH LL-100

    FDA Adverse Event
    Injury ·WALLACH SURGICAL DEVICES, INC.·Product code GEH·March 14, 2002

    WALLACH INSEMINATOR

    FDA Adverse Event
    Malfunction ·WALLACH SURGICAL DEVICES, INC.·Product code MFD·October 10, 2007

    WALLACH FREEZER

    FDA Adverse Event
    Injury ·WALLACH SURGICAL DEVICES, INC.·Product code HQA·December 26, 1995

    PAPETTE

    FDA Adverse Event
    Other ·WALLACH SURGICAL DEVICES, INC.·Product code HFE·May 4, 2004

    PAPETTE

    FDA Adverse Event
    Other ·WALLACH SURGICAL DEVICES, INC.·Product code HHT·April 1, 2003

    WALLACH PAPETTE CERVICAL CELL SAMPLER

    FDA Adverse Event
    Malfunction ·WALLACH SURGICAL DEVICES, INC.·Product code HHT·August 14, 2007

    PAPETTE

    FDA Adverse Event
    Malfunction ·WALLACH SURGICAL DEVICES, INC.·Product code HHT·July 6, 2007

    CRYOSURGERY UNIT

    FDA Adverse Event
    Malfunction ·WALLACH SURGICAL DEVICES, INC.·Product code GEH·November 4, 1999

    PAPETTE

    FDA Adverse Event
    Malfunction ·WALLACH SURGICAL DEVICES INC·Product code MCO·August 30, 2016

    Wallach Cryotip T-00337 Anorectal Tip used with the Cryosurgical LL100 or LL50X Cryosurgical Systems Reference: 900218

    FDA Recall
    Terminated ·Wallach Surgical Devices, Inc.·Product code GEH·June 6, 2007

    Wallach Cryotip T-00337 Anorectal Tip, Teflon Coated, used with the Cryosurgical LL100 or LL50X Reference: 900220

    FDA Recall
    Terminated ·Wallach Surgical Devices, Inc.·Product code GEH·June 6, 2007

    Q2000 ELECTROSURGICAL GENERATOR

    FDA Adverse Event
    Injury ·COOPERSURGICAL, INC., ALSO TRADING AS WALLACH SURGICAL DEVICES·Product code GEI·April 12, 2011

    LL100 CRYO FRZ NO GAS

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code GEH·November 11, 2022

    LL100 CRYOSURGICAL

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code GEH·January 24, 2022

    LL100 CRYOSURGICAL

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code GEH·July 22, 2022

    LL100 CRYOSURGICAL

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code GEH·July 29, 2022

    LL100 CRYOSURGICAL

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code GEH·September 8, 2022

    LL100 CRYOSURGICAL

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code GEH·August 24, 2022

    LL100 CRYOSURGICAL

    FDA Adverse Event
    Malfunction ·COOPERSURGICAL, INC.·Product code GEH·February 1, 2022

    Wallace Artificial Insemination Catheter, 180 mm, Sterile, Quantity: 1 Box (10 units), Model: AIC18JP, Cooper Surgical Inc., (01) 2 0888937 021749 - Product Usage: Intended use of the product is the introduction of washed spermatozoa into the uterine cavity.

    FDA Recall
    Terminated ·CooperSurgical, Inc.·Product code MFD·February 28, 2020