BEUDAMED
    1,176 results · 21ms · Sources: EU EUDAMED, US FDA

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    NEU_INS_STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·June 13, 2012

    NEU_INS_STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·June 13, 2012

    NEPHRETECT

    FDA Adverse Event
    Other ·ALDEN SCIENTIFIC, INC.·Product code HZT·August 30, 1996

    NEPHRETECT

    FDA Adverse Event
    Other ·ALDEN SCIENTIFIC, INC.·Product code HZT·July 23, 1999

    NEPHRETECT

    FDA Adverse Event
    Injury ·ALDEN, A DIV OF METREX RESEARCH CORP·Product code HZT·May 17, 2001

    Histochemical PAS (Periodic Acid Schiff) Reaction Set' Class I, IVD; Set of 4 bottles including Schiff Reagent 225 mL, Light Green SF Yellowish Stain 225 mL, Sodium Carbonate Solution 225 mL and Periodic Acid Solution 225 mL' EMD Chemicals, Inc. 480 S. Democrat Road, Gibbstown, NJ 08027 Each kit provides reagents sufficient for a maximum of 100 tests.

    FDA Recall
    Terminated ·EMD Chemicals Inc·Product code HZT·June 2, 2008

    Schiff Reagent, Hotchkiss-McManus, packaged in an amber glass bottle with a black polypropylene cap.

    FDA Recall
    Open, Classified ·EMD Millipore Corporation·Product code HZT·January 26, 2024

    Reagent, Schiff

    FDA classification
    FDA Class 1 ·Reagent, Schiff

    HMT MICROELECTRONIC AG

    FDA registration
    HMT MICROELECTRONIC AG·1 product·🇨🇭 Switzerland

    HMT Medizintechnik GmbH

    FDA registration
    HMT Medizintechnik GmbH·2 products·🇩🇪 Germany

    CZT Upgrade

    FDA UDI
    G E MEDICAL SYSTEMS ISRAEL LTD.·00840682141635·

    PRINTEC H.T. ELECTRONICS CORP.

    FDA registration
    PRINTEC H.T. ELECTRONICS CORP.·4 products·🇹🇼 Taiwan

    D670 CZT Upgrade

    FDA UDI
    G E MEDICAL SYSTEMS ISRAEL LTD.·00840682123778·

    Discovery NM/CT 670 CZT

    FDA 510(k)
    FDA Class 2 ·Radiology

    Foshan HCT Medical Equipment Co.,Ltd

    FDA registration
    Foshan HCT Medical Equipment Co.,Ltd·4 products·🇨🇳 China

    Discovery NMCT 670 CZT

    FDA UDI
    G E MEDICAL SYSTEMS ISRAEL LTD.·00840682121446·

    GIOTTO HIGH TECH (H.T.) MAMMOGRAPHIC SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    870DR to 870 CZT Upgrade

    FDA UDI
    G E MEDICAL SYSTEMS ISRAEL LTD.·00840682145725·

    SUDS HIV-1

    FDA Adverse Event
    Other ·MUREX DIAGNOSTICS·Product code LRM·October 4, 2000

    HEALTH TRONICS LITHOTRON

    FDA Adverse Event
    Injury ·HMT·Product code LNS·August 2, 2004