BEUDAMED
    11 results · 19ms · Sources: EU EUDAMED, US FDA

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    STERILE CATHERIZATION PROCEDURE TRAYS

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    iNSitu Hip System

    FDA UDI
    NEXTSTEP ARTHROPEDIX, LLC·00816127025969·Acetabular Reamer, Full Hemisphere, Crossbar, 59mm

    KD-726 MEMORY WRIST AUTOMATIC ELECTRONIC BLOOD PRESSURE MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CAPIOX SX18 HOLLOW FIBER OXYGENATOR WITH DETACHABLE HARDSHELL RESERVOIR, CAPIOX SX25 HOLLOW FIBER OXGENATOR WITH DETACHA

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ULTRA-THIN SDS BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code DQY·December 13, 2006

    5MM RETRIEVAL SYSTEM

    FDA Adverse Event
    Malfunction ·APPLIED MEDICAL·Product code GCJ·May 23, 2014

    UNKNOWN DEPUY PE CUP

    FDA Adverse Event
    Injury ·DEPUY FRANCE·Product code HSD·November 13, 2012

    LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER 20 MEDIUM-LARGE TITANIUM LIGA

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code FZP·January 10, 2008

    Clarity Precision Grip Attachments, for use in orthodontic treatment. Part numbers/SKUs: 359-830 359-831 359-832 359-833 359-834 359-835 359-836 359-837

    FDA Enforcement
    Class II ·Ongoing·3M Company - Health Care Business·January 1, 2025

    Clarity Precision Grip Attachments, for use in orthodontic treatment. Part numbers/SKUs: 359-830 359-831 359-832 359-833 359-834 359-835 359-836 359-837

    FDA Recall
    Open, Classified ·3M Company Health Care Business 3m Center·Product code NXC·November 22, 2024

    Daig Livewire Steerable, Product Number 401575; REPROCESSED ELECTROPHYSIOLOGY CATHETER

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