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

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    BODY POSITION INDICATOR, MODEL BPI1

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    VARIAX

    FDA UDI
    Stryker GmbH·04546540704115·Plate Trial Insert

    KENAFLEXX

    FDA UDI
    KENTRON HEALTHCARE, INC.·00810003750082·12" IV EXTENSIO SET WITH FEMALE LUER CONNECTOR,...

    SIGMA

    FDA UDI
    DEPUY (IRELAND)·10603295223399·SIGMA FEMORAL CRUCIATE RETAINING POROCOAT SIZE ...

    Lenses, Soft Contact, Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·PRECISION(TM) UV (VASURFILCON)

    SOPIX INSIDE, SOPIX2 INSIDE

    FDA 510(k)
    FDA Class 2 ·Dental

    ANGIOJET XPEEDIOR 120 CATHETER AND ANGIOJET POWER PULSE SPRAY ANCILLARY KIT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Lenses, Soft Contact, Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·PRECISION(TM) UV (VASURFILCON)

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·PRECISION(TM) UV (VASURFILCON)

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·PRECISION(TM) UV (VASURFILCON)

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·PRECISION(TM) UV (VASURFILCON)

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·PRECISION(TM) UV (VASURFILCON)

    Lenses, Soft Contact, Daily Wear

    FDA Pre-Market Approval
    FDA Class 2 ·PRECISION ULTRAVIOLET (VASURFILCON A) HYDROPHILIC CONTACT LENS FOR EXTENDED WEAR

    Lenses, Soft Contact, Extended Wear

    FDA Pre-Market Approval
    FDA Class 3 ·CIBA VISION (VASURFILCON A) SOFT CONTACT LENSES

    GUARDIAN REAL-TIME MONITIOR

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code MDS·February 1, 2013

    ADULT INSPIRATORY HEATED BREATHING CIRCUIT

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BTT·December 28, 2010

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 17, 2014

    SIG C/R POROCOAT FEM LT SZ 3

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code MBH·April 8, 2009

    DEPUY CMW 2 20G

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LOD·November 5, 2019

    Captus 4000e Thyroid Uptake System, Model Numbers 5430-30151 and 5430-30152 - Product Usage: is intended to be used by trained nuclear Medicine Technologists or Nuclear Medicine Physicians to perform Thyroid Uptake Procedures.

    FDA Enforcement
    Class II ·Terminated·Capintec Inc·April 1, 2020