BEUDAMED
    76 results · 24ms · Sources: EU EUDAMED, US FDA

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    Aesculap Miethke Shunt System, miniNAV Valve: The Miethke Shunt System is intended to shunt cerebrospinal fluid (CSF) from the lateral ventricles of the brain into the peritoneum.

    FDA Enforcement
    Class III ·Terminated·Aesculap, Inc.·December 24, 2014

    Aesculap Inc.(AIC) Miethke Ventricular Catheter with Deflector/Miethke Shunt System The Miethke Shunt System is intended to shut cerebrospinal fluid from the lateral ventricles of the brain into the peritoneum.

    FDA Enforcement
    Class II ·Terminated·Aesculap, Inc.·June 11, 2014

    Columbus Revision Knee System, EnduRo Knee System Product Usage: The Columbus Revision Knee System and EnduRo Knee System are indicated for use in reconstruction of the diseased knee joint.

    FDA Enforcement
    Class II ·Terminated·Aesculap, Inc.·March 9, 2016

    The Dual Switch Valve is used for fluid drainage from the ventricles into the peritoneum, in cases of hydrocephalus.

    FDA Enforcement
    Class II ·Terminated·Aesculap, Inc.·December 10, 2014

    Dafilon Suture Black 10/0 (0.2) 15 cm DRM4 NS, non-sterile, non-absorbable polyamide Surgical Suture, additional label affixed on the box states the product is sterile, packaged in a cassette holding 12 sutures

    FDA Enforcement
    Class II ·Terminated·Aesculap, Inc.·July 16, 2014

    Aesculap Miethke Shunt System, miniNAV Valve: The Miethke Shunt System is intended to shunt cerebrospinal fluid (CSF) from the lateral ventricles of the brain into the peritoneum.

    FDA Recall
    Terminated ·Aesculap, Inc.·Product code JXG·November 11, 2014

    Excia Cemented Hip Stems, Size 12mm, Part Number: NJ312K, Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    Excia Cemented Hip Stems, Size 17mm, Part Number : NJ317K, Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    Excia Cemented Hip Stems, Size 14mm, Part Number : NJ314K, Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    Excia Cemented Hip Stems ,Size 18mm, Part Number NJ318K, Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    Excia Cemented Hip Stems, Size 13mm, Part Number : NJ313K, Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    Excia Cemented Hip Stems, Size 16mm, Part Number NJ316K, Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    Excia Cemented Hip Stems, Size 9mm, Part Number: NJ309K, Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    Excia Cemented Hip Stems, Size 11mm, Part Number : NJ311K, Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    Excia Cemented Hip Stems, Size 10mm, Part Number: NJ310K, Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    Excia Cemented Hip Stems, Size 15mm, Part Number: NJ315K Aesculap Implant Systems, Inc., Center Valley, PA 18034

    FDA Recall
    Terminated ·Aesculap Implant Systems·Product code LWJ·October 10, 2007

    AESCULAP MINOP InVent 30 Trocar System, non-sterile Product Usage:The Minop InVent Trocar System intended use is for endoscopic procedures within the central nervous system, especially for the treatment of intra- and paraventricular pathological structures.

    FDA Recall
    Terminated ·Aesculap Implant Systems LLC·Product code GWG·March 7, 2017

    Aeos Robotic Digital Microscope with software versions 2.7 or earlier Article Number: PV010

    FDA Recall
    Terminated ·Aesculap Implant Systems LLC·Product code FSO·July 14, 2022

    Flexible Screw Driver SJ706R; Non Sterile; B Braun; Aesculap; Aesculap AG These instruments are intended for use during the implantations of the A-Space SIBD and Arcadius XP L systems.

    FDA Recall
    Terminated ·Aesculap, Inc.·Product code LRZ·November 10, 2015

    Flexible Bone Awl; SJ607R; NON STERILE; B Braun Aesculap; Aesculap AG: These instruments are intended for use during the implantations of the A-Space SIBD and Arcadius XP L systems.

    FDA Recall
    Terminated ·Aesculap, Inc.·Product code LRZ·November 10, 2015