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    EM DEVICE LAB, INC.

    FDA registration
    EM DEVICE LAB, INC.·1 product·🇺🇸 United States

    ACCUMAX LAB DEVICES PVT LTD

    FDA registration
    ACCUMAX LAB DEVICES PVT LTD·7 products·🇮🇳 India

    BreathID Hp Lab Device

    FDA UDI
    MERIDIAN BIOSCIENCE ISRAEL LTD·07290016923384·The BreathID® Hp Lab System is intended for use...

    SALTER LABS PEP DEVICE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Quickloop Abscess Treatment Device

    FDA UDI
    Em Device Lab, Inc·B762M01000010·Device for draining and irrigating cutaneous an...

    BreathID Hp Lab Device (WIN)

    FDA UDI
    MERIDIAN BIOSCIENCE ISRAEL LTD·07290016923391·The BreathID® Hp Lab System is intended for use...

    SURESTEP

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code NBW·November 14, 2005

    VALLEY LAB ELECTROCAUTERY DEVICE

    FDA Adverse Event
    Other ·VALLEYLAB/DIVISION OF TYCO HEALTHCARE GROUP·Product code GEI·May 26, 2004

    CHEMO-SITE

    FDA Adverse Event
    Injury ·DEVICE LABS·Product code LLD·March 1, 1995

    FASTTAKE

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CFR·March 12, 2004

    OT VERIO FLEX METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 6, 2017

    CHEMOSITE

    FDA Adverse Event
    Injury ·DEVICE LABS, INC.·Product code LJT·August 7, 1996

    CHEMOSITE VENOUS ACCESS SYSTEM

    FDA Adverse Event
    DEVICE LABS, INC.·Product code LJT·January 8, 1995

    CHEMOSITE VENOUS ACCESS SYSTEM

    FDA Adverse Event
    DEVICE LABS, INC.·Product code LJT·January 8, 1995

    CHEMOSITE VENOUS ACCESS SYSTEM

    FDA Adverse Event
    DEVICE LABS, INC.·Product code LJT·January 8, 1996

    TRIAGE CARDIAC PANEL 25 TEST

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO INC·Product code MMI·April 12, 2012

    OT VERIO2 METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 17, 2015

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 25, 2015

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 24, 2015

    ONE TOUCH BASIC ENHANCED

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code NBW·November 14, 2005