BEUDAMED
    26 results · 25ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    DAILIES TOTAL DALIES TOTAL FOR ASTIGMATISM DAILIES TOTAL MULTIFOCAL DAILIES TOTAL MULTIFOCAL TORIC

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    Thread Cleaner M6

    FDA UDI
    Noras MRI products GmbH·04251269200816·

    Nautilus Spinal System

    FDA UDI
    Life Spine, Inc.·00190837052478·

    IMUBIND PLASMA PAI-1 ELISA,MODEL 822

    FDA 510(k)
    FDA Class 2 ·Hematology

    B-CARE5 (B-CARE5 SENSOR MODULE, VENOUS SENSOR, HOLDER FOR MEASURING HEAD)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ONE TOUCH PROFILE

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·April 29, 2002

    OT VERIO FLEX METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 7, 2017

    REMSTAR AUTO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·August 20, 2021

    REMSTAR PRO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·August 20, 2021

    REMSTAR AUTO A-FLEX W/HUMID

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code BZD·August 10, 2021

    REMSTAR AUTO A-FLEX, SYS ONE, 60 SRS, FR

    FDA Adverse Event
    Injury ·RESPIRONICS, INC·Product code BZD·August 5, 2021

    REMSTAR AUTO A-FLEX, SYS ONE, 60 SRS,GER

    FDA Adverse Event
    Injury ·RESPIRONICS INC·Product code BZD·August 30, 2021

    VILEX

    FDA Adverse Event
    Malfunction ·VILEX, INC.·Product code JDW·June 4, 2012

    REMSTAR PRO C-FLEX+

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC·Product code BZD·February 8, 2022

    DUAL COOLER/HEATER

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DWC·May 9, 2013

    ONCOTYPE DX MULTIVARIATE INDEX

    FDA Adverse Event
    Injury ·GENOMIC HEALTH·Product code NPQ·May 27, 2011

    UNKNOWN PAINPUMP PRODUCT

    FDA Adverse Event
    Injury ·STRYKER INSTRUMENTS, KALAMAZOO·Product code MEB·August 12, 2008

    REMSTAR PRO C-FLEX+

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC·Product code BZD·February 8, 2022

    REMSTAR AUTO A-FLEX

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code BZD·January 14, 2022

    REMSTAR AUTO A-FLEX W/SD CARD, GER

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC·Product code BZD·August 5, 2021