BEUDAMED
    50 results · 31ms · Sources: EU EUDAMED, US FDA

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    Profound Matrix

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

    Comprehensive® SRS

    FDA UDI
    Biomet Orthopedics, LLC·00880304522732·

    10PW - Penn Power & Light

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588012179·10PW - Penn Power & Light

    PMT® Halo Systems

    FDA UDI
    PMT CORPORATION·00650551112280·HALO, 1203-5 VEST MEDIUM, LAMBSWOOL LINER, 1211...

    CLEAR OR BRAIDED CONTRAST MEDIA INJECTION LINE WITH OR WITHOUT ROTATOR, CATH LAB KIT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ADDITIVE CAP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·May 25, 2023

    UNKNOWN CYPHER JAPAN

    FDA Adverse Event
    Death ·CORDIS CORPORATION·Product code NIQ·February 13, 2018

    UNKNOWN CYPHER JAPAN

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code NIQ·February 13, 2018

    UNKNOWN CYPHER JAPAN

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code NIQ·February 13, 2018

    ARCTIC FRONT ADVANCE CARDIAC CRYOABLATION CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC CRYOCATH LP·Product code OAE·September 2, 2015

    FLEXCATH ADVANCE STEERABLE SHEATH

    FDA Adverse Event
    Injury ·MEDTRONIC CRYOCATH LP·Product code DRA·September 2, 2015

    ARCTIC FRONT ADVANCE CARDIAC CRYOABLATION CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC CRYOCATH LP·Product code OAE·September 2, 2015

    ARCTIC FRONT ADVANCE CARDIAC CRYOABLATION CATHETER

    FDA Adverse Event
    Injury ·MEDTRONIC CRYOCATH LP·Product code OAE·September 2, 2015

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 5, 2025

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 22, 2024

    UNKNOWN CYPHER JAPAN

    FDA Adverse Event
    Injury ·CORDIS CASHEL·Product code NIQ·February 13, 2018

    UNKNOWN CYPHER JAPAN

    FDA Adverse Event
    Injury ·CORDIS CASHEL·Product code NIQ·February 13, 2018

    UNKNOWN CYPHER JAPAN

    FDA Adverse Event
    Injury ·CORDIS CASHEL·Product code NIQ·February 13, 2018

    UNKNOWN CYPHER JAPAN

    FDA Adverse Event
    Injury ·CORDIS CASHEL·Product code NIQ·February 13, 2018