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

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    iHealth BP3L Wireless Blood Pressure Monitor

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LACTOSORB* 2.0MM SYSTEM

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036053918·

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707013839·CALIBRA 1ST MOL BANDS W/G8325-02 n.UR 3

    Geneva

    FDA UDI
    Nucletron B.V.·08717213055957·Ovoid Tube 1 - Interstitial Ovoid 13mm

    ORTHOPEDIATRICS BLADE PLATE SYSTEM

    FDA Adverse Event
    Injury ·ORTHOPEDIATRICS·Product code HRS·October 3, 2017

    Liner Impactor

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215039325·

    Staple Shaft

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215165284·

    Signature Femoral Head

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215017903·

    VNUS RFS, MODEL RFS-6-XX (XX = 10, 12, 13, & 15); VNUS RFS FLEX, MODEL RFX-6-XX (XX = 10, 20, 30 & 40)

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    XPRESS BALLOON DEVICE

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    Herbert/Whipple®

    FDA UDI
    Zimmer, Inc.·00889024033757·

    BINAXNOW COVID-19 ANTIGEN SELF TEST

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC·Product code QKP·April 5, 2022

    BINAX NOW COVID-19 SELF TEST

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·June 8, 2021

    SYNCHROMED

    FDA Adverse Event
    Other ·NEURO·Product code LKK·October 31, 2003

    CLINITRON RITE HITE

    FDA Adverse Event
    Injury ·HILL-ROM MANUFACTURING, INC.·Product code INX·October 17, 2003

    VITALITY VR

    FDA Adverse Event
    Malfunction ·CARDIAC PACEMAKERS, INC·Product code LWS·August 10, 2005

    STRETTA SYSTEM

    FDA Adverse Event
    Other ·CURON MEDICAL, INC.·Product code JOS·June 16, 2003

    BINAX NOW COVID-19 AG CARD

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QKP·August 15, 2021

    VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·November 18, 2019

    HALL SURGICAL

    FDA Adverse Event
    Injury ·LINVATEC CORPORATION·Product code HTT·March 3, 2006