BEUDAMED
    25 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 ×

    Kindguard Powder Free Vinyl Patient Examination Gloves, Light Yellow Color

    FDA 510(k)
    FDA Class 1 ·General Hospital

    HORICO

    FDA UDI
    Hopf, Ringleb & Co. GmbH & Cie.·EHORW1730162·Rotary diamond instrument

    Endo Stitch

    FDA UDI
    Covidien LP·10884521100008·Suturing Device

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694027397·3.0mm X 16mm Cannulated Headless Screw

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668108901·BURNSTINE LACRIMAL CANNULA

    HORICO

    FDA UDI
    Hopf, Ringleb & Co. GmbH & Cie.·EHORFG1730165·Rotary diamond instrument

    HORICO

    FDA UDI
    Hopf, Ringleb & Co. GmbH & Cie.·EHORFG1730162·Rotary diamond instrument

    FG Dental Burs

    FDA UDI
    BIOLINE DENTAL IMPLANT SYSTEMS LTD·07290119311675·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694069304·Cannulated 3.0 x 16mm Headless Screw Sterile Qty 5

    VERI-Q SELF-TESTING AND VERI-Q PLUS MGD-2001 BLOOD GLUCOSE MONITORING SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    TROJAN THINTENSITY BRAND MALE LATEX CONDOM LUBRICATED WITH ULTRASMOOTH AND WARM SENSATIONS LUBRICANT

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    V-LOC 180

    FDA Adverse Event
    Injury ·COVIDIEN LP LLC NORTH HAVEN·Product code GAM·September 16, 2022

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·July 23, 2011

    GYNECARE PROLIFT PELVIC FLOOR REPAIR SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTP·June 17, 2013

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 19, 2008

    173016 @ENDO STITCH 10 MM SUTURING DEVIC

    FDA Adverse Event
    Injury ·MEDLINE INDUSTRIES LP·Product code HCF·November 23, 2021

    173016 @ENDO STITCH 10 MM SUTURING DEVIC

    FDA Adverse Event
    Injury ·MEDLINE RENEWAL·Product code GAM·February 1, 2023

    173016 @ENDO STITCH 10 MM SUTURING DEVIC

    FDA Adverse Event
    Injury ·MEDLINE RENEWAL·Product code HCF·December 17, 2024

    173016 @ENDO STITCH 10 MM SUTURING D

    FDA Adverse Event
    Injury ·MEDLINE RENEWAL·Product code HCF·April 15, 2025

    ENDO STITCH

    FDA Adverse Event
    Malfunction ·DAVIS & GECK CARIBE LTD·Product code OCW·April 10, 2022