BEUDAMED
    23 results · 21ms · Sources: EU EUDAMED, US FDA

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    STOCKERT CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAMP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SCP PANEL CENTRIFUGE JMS

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DWA·November 5, 2013

    SCP PANEL CENTRIFUGE JMS

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DWA·March 14, 2014

    SCP CONTROL PANEL

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·January 5, 2012

    CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAMP

    FDA Adverse Event
    Malfunction ·LIVANOVA DEUTSCHLAND·Product code DWA·January 19, 2018

    CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAMP

    FDA Adverse Event
    Malfunction ·LIVANOVA DEUTSCHLAND GMBH·Product code DWA·January 5, 2022

    STOCKERT JMS CENTRIFUGAL PUMP SYSTEM

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·January 5, 2012

    STOCKERT CENTRIFUGAL PUMP (SCP) SYSTEM

    FDA Adverse Event
    Injury ·SORIN GROUP DEUTSCHLAND·Product code DWA·May 7, 2010

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04051526785502·M4S COMFORT COMPACT BLACK LEFT M

    Baltic Denture System BD Load

    FDA UDI
    Merz Dental GmbH·D7091032213·Baltic Denture System BDLoad ↓ Mn6 PLSEum2DFm A...

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707067214·LIGATURES MINI modules TRANSP MEDIUM

    Battalion

    FDA UDI
    ALPHATEC SPINE, INC.·00840967187617·Battalion, LLIF Trial, 15°, 22 mm Wide, 13 mm X...

    GULLIVER AND CLASSE A

    FDA 510(k)
    FDA Class 1 ·Dental

    BULL'S-EYE DISPOSABLE NEEDLE RECAPPING AID

    FDA 510(k)
    FDA Class 2 ·General Hospital

    XORAN

    FDA Adverse Event
    Malfunction ·XORAN TECHNOLOGIES, INC.·Product code JAK·May 9, 2011

    S4 IMPLANTS

    FDA Adverse Event
    Malfunction ·AESCULAP AG & CO. KG·Product code KWP·August 29, 2008

    CARE ASSIST BED

    FDA Adverse Event
    Malfunction ·HILL-ROM PLUVIGNER·Product code FNL·March 6, 2013

    UROPASS URETERAL ACCESS SHEATH

    FDA Adverse Event
    Malfunction ·GYRUS ACMI·Product code KNY·March 3, 2011

    60" EXT W/M/FLL CLAMP

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FPA·April 18, 2008

    Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026