BEUDAMED
    870 results · 22ms · 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 ×

    Muscular Dystrophy Newborn Screening Test

    FDA classification
    FDA Class 2 ·Muscular Dystrophy Newborn Screening Test

    Quantum

    FDA UDI
    SPECTRUM MEDICAL LIMITED·05060434420817·Quantum Diagnostic Exhaust for use with Quantum...

    Measles (Rubeola) Antigen Control Slide, 2 wells

    FDA UDI
    Bion Enterprises, Ltd.·B110QME60020·

    Quasar MED IE (QIE) Limited

    FDA registration
    Quasar MED IE (QIE) Limited·1 product·🇮🇪 Ireland

    QA-ES

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

    Subdural Electrode

    FDA UDI
    Ad-Tech Medical Instrument Corporation·00841823103321·

    QUINTON Q-TE; RMS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Welch Allyn, Inc.

    FDA UDI
    WELCH ALLYN, INC.·00732094264197·H3+ 3-channel digital Holter Recorder - 7-day, ...

    ENDOPATH SUBCU-DISSECTOR

    FDA Adverse Event
    Injury ·LACEY MANUFACTURING CO.·Product code GDI·January 14, 1997

    ENDOPATH SUBCU-RETRACTOR

    FDA Adverse Event
    Injury ·LACEY MANUFACTURING CO.·Product code GAD·January 14, 1997

    JE 2000

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    K-QUE-ACT-004 REV002

    FDA UDI
    Quest Diagnostics·00850054552082·QCard Collection Kit

    K-QUE-ACT-007 REV000

    FDA UDI
    Quest Diagnostics·00850054552112·QCard Collection Kit (WHS)

    K-QUE-ACT-001 REV002

    FDA UDI
    Quest Diagnostics·00850054552068·QCard Blood Collection Kit (WHS)

    K-QUE-ACT-003 REV002

    FDA UDI
    Quest Diagnostics·00850054552075·QCard Collection Kit (WHS)

    K-QUE-ACT-006 REV001

    FDA UDI
    Quest Diagnostics·00850054552105·QCard Collection Kit (WHS)

    K-QUE-KED-001 REV000

    FDA UDI
    Quest Diagnostics·00850054552129·QCard Collection Kit

    K-QUE-ACT-005 REV002

    FDA UDI
    Quest Diagnostics·00850054552099·QCard Collection Kit (WHS)

    OPTI [QUE] BALLOON

    FDA Adverse Event
    Other ·ABBOTT LABORATORIES·Product code DQO·January 2, 2004

    C-QUE MESH

    FDA Adverse Event
    Injury ·ATRIUM MEDICAL CORP.·Product code FTL·September 11, 2014