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

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    Hepatitis A Test (Antibody And Igm Antibody)

    FDA Pre-Market Approval
    FDA Class 2 ·AB -HAVK

    Hepatitis A Test (Antibody And Igm Antibody)

    FDA Pre-Market Approval
    FDA Class 2 ·ETI-AB-HAVK PLUS

    Hepatitis A Test (Antibody And Igm Antibody)

    FDA Pre-Market Approval
    FDA Class 2 ·DIASORIN ETI-AB-HAVK PLUS

    Hepatitis A Test (Antibody And Igm Antibody)

    FDA Pre-Market Approval
    FDA Class 2 ·AB-HAVK, ETI-AB-HAVK, ETI-AB-HAVK PLUS

    Hepatitis A Test (Antibody And Igm Antibody)

    FDA Pre-Market Approval
    FDA Class 2 ·DIASORIN ETI-AB-HAVK PLUS

    Hepatitis A Test (Antibody And Igm Antibody)

    FDA Pre-Market Approval
    FDA Class 2 ·ETI-AB-HAVK

    Hepatitis A Test (Antibody And Igm Antibody)

    FDA Pre-Market Approval
    FDA Class 2 ·DIASORIN ETI-AB-HAVK PLUS ASSAY

    Hepatitis A Test (Antibody And Igm Antibody)

    FDA Pre-Market Approval
    FDA Class 2 ·AB-HAVK RIA ASSAY/ETI-AB-HAVK PLUS

    ReLine

    FDA UDI
    Nuvasive, Inc.·00195377035165·RELINE-C Bender, Rod

    Trimline

    FDA UDI
    ORMCO CORPORATION·00889989052558·LOWER LEFT SECOND MOLAR TRIMLINE BAND SIZE 19

    LATEX SURGICAL GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    APEX MONORAIL

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code LOX·June 19, 2009

    VerSys®

    FDA UDI
    Zimmer, Inc.·00889024140332·

    APEX MONORAIL

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code LOX·June 8, 2009

    MAVERICK2 MONORAIL PTCA CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code LOX·April 19, 2007

    Drug-Eluting Peripheral Transluminal Angioplasty Catheter

    FDA Pre-Market Approval
    FDA Class 3 ·Ranger™ Paclitaxel-Coated PTA Balloon Catheter

    Hepatitis A Test (Antibody And Igm Antibody)

    FDA Pre-Market Approval
    FDA Class 2 ·HAVAB-M DIAGNOSTIC KIT

    APEX MONORAIL

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code LOX·April 20, 2009

    HEARTSTART XL DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 2, 2014

    ACCU-CHEK SPIRIT

    FDA Adverse Event
    Injury ·ROCHE INSULIN DELIVERY SYSTEMS INC·Product code LZG·November 1, 2010