BEUDAMED
    108 results · 38ms · Sources: EU EUDAMED, US FDA

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    Polarizer D Fixed w/Rotating Red 1 lambda plate. Utilized in upright Zeiss microscopes to aid in diagnosis by means of color variation.

    FDA Enforcement
    Class II ·Terminated·Zeiss, Carl Inc·July 24, 2013

    Compensator Slider Lambda 6x20 component (part number 473704-0000-000) utilized on all upright ZEISS microscopes (Axio Imager, Axio Scope. A1, Axio Lab. A1). Component used to determine composition of urinary calculi, urinary sediments, bio-crystallates and diagnosis of pathological characteristics in medical applications (e.g.: testing for gout or pseudogout); also used for non-medical scientific research.

    FDA Enforcement
    Class II ·Terminated·Zeiss, Carl Inc·January 29, 2014

    Polarizer D Fixed w/Rotating Red 1 lambda plate. Utilized in upright Zeiss microscopes to aid in diagnosis by means of color variation.

    FDA Recall
    Terminated ·Zeiss, Carl Inc·Product code IBJ·May 28, 2013

    Compensator Slider Lambda 6x20 component (part number 473704-0000-000) utilized on all upright ZEISS microscopes (Axio Imager, Axio Scope. A1, Axio Lab. A1). Component used to determine composition of urinary calculi, urinary sediments, bio-crystallates and diagnosis of pathological characteristics in medical applications (e.g.: testing for gout or pseudogout); also used for non-medical scientific research.

    FDA Recall
    Terminated ·Zeiss, Carl Inc·Product code IBJ·December 20, 2013

    ENCOR BIOPSY PROBE, UPRIGHT

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·August 6, 2015

    *

    FDA Adverse Event
    Injury ·*·Product code FWM·August 14, 2006

    9614385-2007-00015

    FDA Adverse Event
    Injury ·Product code FWM·April 12, 2007

    9614385-2006-00058

    FDA Adverse Event
    Injury ·Product code FWM·September 25, 2006

    9614385-2007-00012

    FDA Adverse Event
    Injury ·Product code FWM·April 2, 2007

    9614385-2006-00081

    FDA Adverse Event
    Injury ·Product code FWM·December 4, 2006

    9614385-2006-00073

    FDA Adverse Event
    Injury ·Product code FWM·November 21, 2006

    9614385-2006-00057

    FDA Adverse Event
    Injury ·Product code FWM·September 25, 2006

    9614385-2006-00046

    FDA Adverse Event
    Injury ·Product code FWM·August 9, 2006

    9614385-2006-00085

    FDA Adverse Event
    Injury ·Product code FWM·January 8, 2007

    9614385-2007-00011

    FDA Adverse Event
    Injury ·Product code FWM·April 2, 2007

    9614385-2006-00047

    FDA Adverse Event
    Injury ·Product code FWM·August 9, 2006

    9614385-2007-00006

    FDA Adverse Event
    Injury ·Product code FWM·February 23, 2007

    9614385-2006-00088

    FDA Adverse Event
    Injury ·Product code FWM·January 12, 2007

    *

    FDA Adverse Event
    Injury ·*·Product code FWM·August 1, 2007

    9614385-2007-00002

    FDA Adverse Event
    Injury ·Product code ---·January 22, 2007