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

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    Filters Regulation: Us FDA ×

    Intravascular Extension Sets and Accessories

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DEPUY SYNTHES

    FDA UDI
    Medos International Sàrl·10886705028207·DEPUY SYNTHES VISUALIZATION RECTANGULAR TRAY

    Novo Surgical Inc.

    FDA UDI
    NOVO SURGICAL, INC.·00842331153860·suture wire, stainless steel, 28 gauge

    NEOPLANT IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    HEMASORB Resorbable Hemostatic Bone Putty

    FDA 510(k)
    FDA Unclassified ·Unknown

    THERAPY ABLATION CATHETER

    FDA Adverse Event
    Malfunction ·IRVINE BIOMEDICAL, A ST. JUDE MEDICAL COMPANY·Product code OAD·June 25, 2010

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·September 20, 2024

    CARPENTIER-EDWARDS PHYSICO ANNULOPLASTY RING

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code KRH·November 21, 2008

    HOMECHOICE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·September 10, 2011

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·July 23, 2013

    INSPIRA SMOOTH SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·September 25, 2025

    EXPEDIUM VERSE SPINE SYSTEM VERSE CORRECTION KEY 5.5

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SàRL CH·Product code KWQ·March 13, 2020

    VERSE CORRECTION KEY

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SàRL CH·Product code KWQ·March 13, 2020