BEUDAMED
    34 results · 22ms · Sources: EU EUDAMED, US FDA

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    CLASSIC/HYPOTHERMIA, FLEXIBLE, 10-SECOND, LEFT-RIGHT HANDED, BASAL, LIGHTWEIGHT-PROBE DIGITAL CLINICAL THERMOMETER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Paltop

    FDA UDI
    PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290114690157·Open Tray Multi-Unit Impression Coping Screw UN...

    Paltop

    FDA UDI
    PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290108690460·Titanium Anatomic Angulated Abutment Internal H...

    CosmoLock

    FDA UDI
    Kalitec Direct LLC·B073DRK0100280·Tab Breaker, Single Sided, Cosmolock MIS

    Intess C

    FDA UDI
    Kalitec Direct LLC·B07309K0100280·Caddie Lid, Cervical Implants, Hinged

    Navagio

    FDA UDI
    Kalitec Direct LLC·B07330K0100280·Caddie, 32-36mm Curved Cages

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07310K0100280·Caddie, MIS Rods and Caps

    RENAFLO II HF 2000 HEMOFILTER

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    SHEER THIN AROMAS RED LATEX CONDOM

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    LUMOS VR-T

    FDA Adverse Event
    Injury ·BIOTRONIK GMBH AND CO.·Product code LWS·February 20, 2007

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·March 25, 2025

    QUILL SRS

    FDA Adverse Event
    Malfunction ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·September 3, 2008

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORPORATION (DBA ANGIOTECH)·Product code NEW·May 12, 2009

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·February 13, 2009

    PELVREDUCFORCEPS ANGL Ø6.5 L200

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HTD·April 22, 2013

    COULTER LH 500 HEMATOLOGY ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·September 8, 2014

    COBAS INTEGRA 800

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·July 3, 2008

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP (DBA ANGIOTECH)·Product code NEW·March 15, 2010

    QUILL SRS

    FDA Adverse Event
    Other ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·August 24, 2009

    QUILL KNOTLESS TISSUE-CLOSURE DEVICE

    FDA Adverse Event
    Injury ·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·May 11, 2011