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

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    COMEN MULTI-PARAMETER PATIENT MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    EZS05 CLEANING AND DISINFECTING SOLUTION, BAUSCH + LOMB EZS05 CLEANING AND DISINFECTING SOLUTION

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    HIGH GOLD PALLADIUM FREE CERAMIC SOLDER

    FDA 510(k)
    FDA Class 2 ·Dental

    BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAVED KIT

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·April 12, 2024

    SILK SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAP·December 24, 2008

    SILK SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAP·December 24, 2008

    SILK SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAP·December 24, 2008

    SILK SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAP·December 24, 2008

    SILK SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAP·December 24, 2008

    SILK SUTURE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GAP·December 24, 2008

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 14, 2013

    PERSONA CR FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER ORTHOPEDIC MFG LTD·Product code JWH·September 17, 2014

    THERMOTEK

    FDA Adverse Event
    Injury ·Product code ILO·May 27, 2011

    14 SHIDEN HP

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·September 26, 2024

    14 SHIDEN HP

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·February 4, 2025

    14 SHIDEN HP

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·February 13, 2025

    BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAVED KIT

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·April 24, 2024

    BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAVED KIT

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON MEDICAL DEVICES CO., LTD. SUZHOU·Product code PSZ·January 22, 2024

    14 SHIDEN HP

    FDA Adverse Event
    Injury ·KANEKA CORPORATION·Product code LIT·June 20, 2025

    KIT FLU VERITOR SYSTEM 30 TEST JAPAN

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·March 1, 2022