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

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    Filters Regulation: Us FDA ×

    POST OP SPONGE

    FDA 510(k)
    FDA Unclassified ·Unknown

    WELLS LAMONT HANDAGES/MED WRAP DRESSINGS

    FDA 510(k)
    FDA Class 1 ·General Hospital

    LD 400

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    UNSPECIFIED ENDOTRACH TUBE

    FDA Adverse Event
    Malfunction ·MMJ SA DE CV (USD)·Product code BTR·February 9, 2022

    POWER PRO AMBULANCE COT

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FPO·January 30, 2013

    SOLETRA

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code MHY·December 3, 2010

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 15, 2014

    UNK - SCREWS: TITANIUM STERNAL FIXATION SYSTEM

    FDA Adverse Event
    Injury ·MEZZOVICO SYNTHES PRODUKTIONS GMBH·Product code HWC·October 22, 2021

    UNK - SCREWS: TITANIUM STERNAL FIXATION SYSTEM

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HWC·October 22, 2021