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

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    Kit, Test, Alpha-Fetoprotein For Neural Tube Defects

    FDA Pre-Market Approval
    FDA Class 3 ·QUANTITOPE 125I AFP KIT AND CONTROL SERUM

    Kit, Test, Alpha-Fetoprotein For Neural Tube Defects

    FDA Pre-Market Approval
    FDA Class 3 ·QUANTITOPE 125I AFP KIT AND CONTROL SERUM

    Kit, Test, Alpha-Fetoprotein For Neural Tube Defects

    FDA Pre-Market Approval
    FDA Class 3 ·QUANTITOPE 125I AFP KIT AND CONTROL SERUM

    Kit, Test, Alpha-Fetoprotein For Neural Tube Defects

    FDA Pre-Market Approval
    FDA Class 3 ·AFP/OB(TM) RIA KIT

    Kit, Test, Alpha-Fetoprotein For Neural Tube Defects

    FDA Pre-Market Approval
    FDA Class 3 ·QUANTITOPE 125I AFP KIT AND CONTROL SERUM

    Keystone Industries

    FDA UDI
    Keystone Industries·H66818000251·Pk/10 Strength Braid Gold

    BaseVac

    FDA UDI
    R. E. Morrison Equipment Inc·D13028000250·2 HVE operation, 2 saliva ejector operation

    Heartline Needle Holder

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896110496·Heartline Needle Holder With Lock 1, 2 X 8, 5 M...

    Trimline

    FDA UDI
    ORMCO CORPORATION·00889989051292·UPPER LEFT FIRST MOLAR TRIMLINE BAND SIZE 25

    Rampart O

    FDA UDI
    SPINEOLOGY INC.·M7402800025·11x35mm Trial

    DINAMAP RESEARCH MONITOR 1245

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Coselgi

    FDA UDI
    Widex A/S·05706069476361·Coselgi Melodia 10 CMe10-CIC (Light beige ) Lef...

    Coselgi

    FDA UDI
    Widex A/S·05706069476750·Coselgi Melodia 5 CMe5-CIC (Light beige ) Left,...

    Coselgi

    FDA UDI
    Widex A/S·05706069475807·Coselgi Melodia 15 CMe15-CIC (Light beige ) Lef...

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·February 17, 2019

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·January 24, 2019

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·May 8, 2014

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·October 17, 2012

    RESTORE PRIME ADVANCED

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LGW·August 12, 2010

    INTERSTIM II

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code EZW·January 20, 2016