BEUDAMED
    8,850 results · 45ms · 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.

    IRIS SCISSORS, CURVED, 4-1/2+SS 410 OR 420

    FDA 510(k)

    QUANTA Flash Ro52 Reagents

    FDA registration
    INOVA DIAGNOSTICS, INC.·3 products·🇺🇸 United States

    OSTEOMARK NTX SERUM EIA

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    SLUMBERGEAR(TM), MODEL MULTIPLE (004, 005, 005, 007)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Stent, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·MULTI-LINK FAMILY OF CORONARY STENT SYSTEMS (CSS)

    QUANTA LITE SS-A 52 ELISA

    FDA 510(k)
    FDA Class 2 ·Immunology

    QUANTA FLASH RO52, QUANTA FLASH RO52 CALIBRATORS, AND QUANTA FLASH RO52 CONTROLS

    FDA 510(k)
    FDA Class 2 ·Immunology

    Syneture

    FDA UDI
    Covidien LP·10884521189591·Custom Suture Pack,(1) 88863256-41;(2) 88863271...

    Kit, Identification, Neisseria Gonorrhoeae

    FDA Pre-Market Approval
    FDA Class 1 ·GONOSTICON DRI-DOT TEST

    Kit, Identification, Neisseria Gonorrhoeae

    FDA Pre-Market Approval
    FDA Class 1 ·GONOCOCCAL PILI ANTIBODY TEST

    Kit, Identification, Neisseria Gonorrhoeae

    FDA Pre-Market Approval
    FDA Class 1 ·GONOSTICON DRI-DOT

    BSS MEDIKAL

    Device
    EU MDD · Eu Md Class 2b ·BSS MEDİKAL BİLGİSAYAR VE İNŞAAT İMALAT SANAYİ DIŞ TİCARET LİMİTED ŞİRKETİ·On the market·1 country

    BSS MEDIKAL

    Device
    EU MDD · Eu Md Class 2b ·BSS MEDİKAL BİLGİSAYAR VE İNŞAAT İMALAT SANAYİ DIŞ TİCARET LİMİTED ŞİRKETİ·On the market·1 country

    Lens, Contact, Orthokeratology, Overnight

    FDA Pre-Market Approval
    FDA Class 3 ·JSZ ORTHOKERATOLOGY (OPRIFOCON A) CONTACT LENSES FOR OVERNIGHT WEAR

    Stent, Coronary

    FDA Pre-Market Approval
    FDA Class 3 ·MULTI-LINK VISION FAMILY OF CORONARY STENT SYSTEMS (CSS)

    SENTIO MMG

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    NEURALMAS

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    AESCULAP, INC.

    FDA registration
    AESCULAP, INC.·3 products·🇺🇸 United States

    Moss Nasal tube

    FDA registration
    Xeridiem Medical Devices·3 products·🇺🇸 United States

    AESCULAP AG

    FDA registration
    AESCULAP AG·3 products·🇩🇪 Germany