BEUDAMED
    44 results · 28ms · Sources: EU EUDAMED, US FDA

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    Zimmer, Inc. Hip Joint Prostheses MR Labeling I

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Conventional Lead Apron .5mm Small 22 X 33

    FDA UDI
    Flow X Ray Corporation·00843696123086·Conventional Lead Apron .5mm Small, Beige

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694057165·2.4mm Angled Locking Screw Block, ICON

    PELICLASS HUMAN IGG SUBCLASS NEPHELOMETRIC IMMAGE KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    WOUND PRO APEX

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    Widex

    FDA UDI
    Widex A/S·05706069735604·Widex BEYOND B-F2 (Cappuccino brown S-220 ) Tel...

    ITREL II

    FDA Adverse Event
    Death ·MEDTRONIC NEUROMODULATION·Product code MHY·September 16, 2008

    ITREL II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·September 17, 2008

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·July 29, 2025

    COLLEAGUE CX VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 20, 2008

    KIMVENT CLOSED SUCTION SYSTEM FOR ADULTS

    FDA Adverse Event
    Injury ·KIMBERLY-CLARK HEALTH CARE·Product code BSY·August 11, 2011

    OT VERIO PRO METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 2, 2013

    INFUSOMAT SPACE

    FDA Adverse Event
    Malfunction ·B. BRAUN MELSUNGEN AG·Product code FRN·July 13, 2011

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·September 30, 2009

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·September 30, 2009

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·September 30, 2009

    UNKNOWN DEEP BRAIN STIMULATOR

    FDA Adverse Event
    Death ·MEDTRONIC NEUROMODULATION·Product code MHY·July 27, 2009

    DEEP BRAIN STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·July 3, 2008

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNKNOWN SIZE)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·September 29, 2009

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·September 30, 2009