BEUDAMED
    8 results · 18ms · Sources: EU EUDAMED, US FDA

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    SINGLE LUMEN EMBOLECTOMY CATHETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PRIMACONNEX RD AND WD ESTHETIC CONTOUR ZI ABUTMENTS

    FDA 510(k)
    FDA Class 2 ·Dental

    Stryker Upper-Face AXS screws and Mid-Face AXS screws

    FDA 510(k)
    FDA Class 2 ·Dental

    ENDOPATH CURVED SCISSORS

    FDA Adverse Event
    Malfunction ·SYMBIOSIS CORP.·Product code KNS·May 22, 1997

    TENSION FREE VAGINAL TAPE

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code OTN·February 21, 2013

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MEDICAL DIV.·Product code FNL·December 30, 2010

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·August 1, 2014

    Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER

    FDA Enforcement
    Class II ·Ongoing·Stryker Sustainability Solutions·May 20, 2026