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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    BENACEL, MODELS C-001, C-002 AND C-005

    FDA 510(k)
    FDA Unclassified ·Unknown

    iTotal® Patella Sizer

    FDA UDI
    Conformis, Inc.·00850268007170·iTotal® 41mm Patella Sizer Reusable Instrument

    Clamp, Hysterectomy, model Z 30.5cm strongly curved

    FDA UDI
    Geister Medizintechnik GmbH·04057034373248·Clamp, Hysterectomy, model Z 30.5cm...

    JEL 15

    FDA 510(k)
    FDA Class 2 ·Dental

    OSTEOSET BVF KIT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OPEN HEART PACK WITHOUT PLEGIOX BEQ-TOP 40010

    FDA Adverse Event
    Malfunction ·DATASCOPE FAIRFIELD·Product code DWE·May 5, 2017

    OPEN HEART PACK WITHOUT PLEGIOX BEQ-TOP 40010

    FDA Adverse Event
    Malfunction ·DATASCOPE FAIRFIELD·Product code DWE·May 5, 2017

    CARDIAC SURGERY PACK BO-TOP 36500

    FDA Adverse Event
    Malfunction ·DATASCOPE FAIRFIELD·Product code DWE·March 28, 2017

    SPECTRA WAVEWRITER?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·November 24, 2025

    CUSTOM TUBING PACK

    FDA Adverse Event
    Malfunction ·DATASCOPE FAIRFIELD·Product code DWE·February 1, 2017

    CUSTOM TUBING PACKS

    FDA Adverse Event
    Malfunction ·DATASCOPE FAIRFIELD·Product code DWE·February 1, 2017

    PASSIVE PLUS DX

    FDA Adverse Event
    Death ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVN·April 26, 2013

    ENDEAVOR SPRINT RX CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC IRELAND·Product code NIQ·April 22, 2011

    ACCU-CHEK COMFORT CURVE TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·July 22, 2008

    BO-TOP 36500 QUADROX OXYGENATOR

    FDA Adverse Event
    Malfunction ·DATASCOPE FAIRFIELD·Product code DWE·November 14, 2017

    CUSTOM TUBING PACK

    FDA Adverse Event
    Malfunction ·DATASCOPE FAIRFIELD·Product code DWE·February 1, 2017

    CUSTOM SURGERY PACK BO-TOP 36500/ QUADROX

    FDA Adverse Event
    Malfunction ·DATASCOPE FAIRFIELD·Product code DWE·September 28, 2017

    BEQ-TOP 5210 ECC PACK

    FDA Adverse Event
    Malfunction ·DATASCOPE FAIRFIELD·Product code DWE·November 9, 2017

    CUSTOM PACK BO-T 25102

    FDA Adverse Event
    Malfunction ·DATASCOPE FAIRFIELD·Product code DWE·March 31, 2017

    CUSTOM TUBING PACK BO TOP 25102

    FDA Adverse Event
    Malfunction ·DATASCOPE FAIRFIELD·Product code DWE·March 31, 2017