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

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    Terragene® Bionova® Hyper Biological Indicator (BT98), Terragene® Bionova® Hyper Auto-reader Incubator (BHY), Terragene® Bionova® NanoBio Auto-reader Incubator (BNB)

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Steril Peel

    FDA UDI
    AMD Medicom Inc·D830221641·STERIL-PEEL Heat Seal Sterilization Pouch Size ...

    BARRIGEL INJECTABLE GEL

    FDA Adverse Event
    Malfunction ·PALETTE LIFE SCIENCES·Product code OVB·June 24, 2024

    XTD THROMBECTOMY CATHETER, XX CM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MINIARC PRO SINGLE-INCISION SLING SYSTEM

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

    UNKNOWN DEPUY 10.5 MMA FEMORAL STEM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.1818910·Product code KWA·November 3, 2014

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·August 24, 2011

    DELTA CER HEAD 12/14 36MM +8.5

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code LZO·July 11, 2013

    SINGLE USE DISTAL COVER

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP. HINODE PLANT·Product code FDT·February 19, 2025