BEUDAMED
    32 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 ×

    CELLVIZIO 100 SERIES SYSTEM AND CELLVIZIO SYSTEM WITH CONFOCAL MINIPROBES

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756612388·Wrist Splint

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04064984699427·GENUMEDI SILVER SIZE VIII

    DURAVENT

    FDA UDI
    Andreas Fahl Medizintechnik-Vertrieb GmbH·04051948006865·DURAVENT XL 2 IC, SIZE 8

    RESTORIS

    FDA UDI
    MAKO SURGICAL CORP.·00848486018115·PIN PULLER

    ARGELITE 61 (5 dwt)

    FDA UDI
    ARGEN CORPORATION, THE·D818120208·Alloy other noble metal

    JOBST soSoft

    FDA UDI
    BSN MEDICAL, INC.·00035664007638·SOSOFT 15-20 MM HG KNEE HIGH BROCADE EXTRA LARG...

    General Instrument

    FDA UDI
    ALPHATEC SPINE, INC.·00840180513606·ALIF, Short Modular Rasped Rotating Distractor,...

    GUTTA PERCHA POINTS

    FDA UDI
    DiaDent Group International·08806383505512·Gutta Percha Points is used to root canal filin...

    Hayden Medical

    FDA UDI
    Hayden Medical, Inc.·00840319739846·Heaney Tissue Forceps 7-1/2" (18.8cm), 1x2 teeth

    ID NOW COVID-19

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·August 20, 2020

    ID NOW COVID-19

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·August 20, 2020

    ID NOW COVID-19

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·August 20, 2020

    ID NOW COVID-19

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·August 20, 2020

    ID NOW COVID-19

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·August 7, 2020

    ID NOW COVID-19

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·August 7, 2020

    ID NOW COVID-19

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·August 20, 2020

    IMC SURGICAL DRAPE

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

    GLUCOMETER ELITE DIABETES CARE SYSTEM (MODIFIED)

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    ID NOW COVID-19

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·September 26, 2020