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

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    ARTIS pheno (VE2)

    FDA 510(k)
    FDA Class 2 ·Radiology

    Integra® Jarit®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780433835·Integra® Jarit® Richardson Retractor, 9-1/2", H...

    Dornier MedTech

    FDA UDI
    DORNIER MEDTECH AMERICA, INC.·04049958003127·400 micron Holmium Laser Fiber Cable, Single Us...

    Corneal Trephine

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112915·CORNEAL TREPHINE BLADE7.5MM

    AVANOS

    FDA UDI
    Avanos Medical, Inc.·00350770456836·CORFLO* Nasogastric/Nasointestinal Feeding Tube

    CORFLO ULTRA Lite NG

    FDA UDI
    CORPAK MEDSYSTEMS, INC.·10815149022960·Feeding tube

    Halyard

    FDA UDI
    Avanos Medical, Inc.·10680651456837·HALYARD* CORFLO* Nasogastric/Nasointestinal Fee...

    PHOENIX HEMODIALYSIS DELIVERY SYSTEM, GAMBRO CARTRIDGE FOR HEMODIALYSIS BLOOD TUBING SET

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

    Bright Low Flow

    FDA 510(k)
    FDA Class 2 ·Dental

    9616240-2006-00341

    FDA Adverse Event
    Malfunction ·Product code FII·June 14, 2006

    9616240-2006-00332

    FDA Adverse Event
    Other ·Product code FII·June 1, 2006

    PHOENIX

    FDA Adverse Event
    Malfunction ·GAMBRO DASCO·Product code FII·May 10, 2006

    9616240-2006-00339

    FDA Adverse Event
    Malfunction ·Product code FII·June 9, 2006

    9616240-2006-00340

    FDA Adverse Event
    Malfunction ·Product code FII·June 9, 2006

    9616240-2006-00350

    FDA Adverse Event
    Malfunction ·Product code FII·June 23, 2006

    9616240-2006-00345

    FDA Adverse Event
    Malfunction ·Product code FII·June 14, 2006

    PHOENIX

    FDA Adverse Event
    Malfunction ·GAMBRO DASCO·Product code FII·May 10, 2006

    PHOENIX

    FDA Adverse Event
    Malfunction ·GAMBRO DASCO·Product code FII·May 10, 2006

    WALLFLEX DUODENAL

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code MUM·January 22, 2025

    AMPLATZER DUCT OCCLUDER

    FDA Adverse Event
    Injury ·AGA MEDICAL CORPORATION·Product code MAE·October 20, 2008