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

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    FIRSTSAVE STAR BIPHASIC, MODEL 9210/9200

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    Mesh

    FDA UDI
    Nuvasive, Inc.·00887517276179·Mesh Titanium Tray, Base

    Port Access Needle

    FDA UDI
    Bard Access Systems, Inc.·00801741065477·HuberPlus 19G x 1"

    ICU Medical

    FDA UDI
    ICU MEDICAL, INC.·00840619023287·ChemoClave™ Vial Spike, 13mm

    STEVE MADDEN

    FDA UDI
    FGX INTERNATIONAL INC.·00193033334102·

    STEVE MADDEN

    FDA UDI
    FGX INTERNATIONAL INC.·00193033334126·

    STEVE MADDEN

    FDA UDI
    FGX INTERNATIONAL INC.·00193033334119·

    Phonak

    FDA UDI
    Phonak AG·07613275113394·Phonak Bolero Q70-SP (beige)

    FIXION INTRAMEDULLARY NAILING SYSTEM (FIXION IMN) MODEL B

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    POLY PER-Q-CATH PICC CATHETER,MODEL 3236100 AND POLY PER-Q-CATH MIDLINE CATHETER, MODEL 3134135

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ULTRA-THIN SDS BALLOON CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code LIT·December 1, 2006

    ULTRA-THIN SDS BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP.·Product code DQY·March 27, 2007

    ULTRA-THIN SDS BALLOON CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code DQY·December 28, 2006

    TI TITAMAX IMPLANT (4.1)3.75X9

    FDA Adverse Event
    Injury ·NEODENT - JJGC S.A.·Product code DZE·May 10, 2018

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·January 14, 2025

    ULTRA-THIN SDS BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORP.·Product code DQY·March 5, 2007

    ULTRA-THIN SDS BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 28, 2006

    ULTRA-THIN SDS BALLOON CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORP.·Product code DQY·April 12, 2007

    SEDLINE EEG SENSOR

    FDA Adverse Event
    Malfunction ·MASIMO - 15750 ALTON PKWY·Product code OLW·February 23, 2026

    PULSE GEN MODEL 1000

    FDA Adverse Event
    Injury ·HOUSTON·Product code LYJ·November 26, 2025