BEUDAMED
    118 results · 29ms · Sources: EU EUDAMED, US FDA

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    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·(POLYMACON) SOF-FORM II CONTACT LENSES

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·(POLYMACON) CONTACT LENSES

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·(POLYMACON) SOF-FORM II CONTACT LENSES

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·(POLYMACON) CONTACT LENSES

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·CELUSOFT (POLYMACON) LENS

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR88200051·Max. 1. Molar band W-Fit left 05

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707027218·WEB 1ST MOLAR BANDS n.UR 5

    CC Anatomic Abutment H5mm L4mm

    FDA UDI
    NOGA MEDICAL PRODUCTS LTD·07290118142096·CC Anatomic Abutment H5mm L4mm

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR88200050501·Max. 1. Molar band W-Fit left 05

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR88200050051·Max. 1. Molar band W-Fit left 05

    Specialty Instrument

    FDA UDI
    Paragon 28, Inc.·00889795146625·MIS Chamfer Screw, 5mm Reduction Wire

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR88200050101·Max. 1. Molar band W-Fit left 05

    TOTAL HEMOLYTIC COMPLEMENT TEST KIT

    FDA 510(k)

    Sensor, Glucose, Invasive

    FDA Pre-Market Approval
    FDA Class 3 ·DEXCOM G4 PLATINUM CONTIUOUS GLUCOSE MONITORING SYSTEM

    Somatic Gene Mutation Detection System

    FDA Pre-Market Approval
    FDA Class 3 ·CRCDx RAS Mutation Detection Assay Kit

    ACRYSOF

    FDA Adverse Event
    Injury ·ALCON RESEARCH, LTD/HUNTINGTON·Product code HQL·May 14, 2014

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·November 5, 2012

    SYNCHRON LXI ACCESS® 2I IMMUNOASSAY CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code MMI·August 30, 2010

    PULSE GENERATOR, PERMANENT, IMPLANTABLE

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVZ·June 9, 2016

    ADAPTA DR

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code NVZ·June 10, 2015