BEUDAMED
    31 results · 31ms · Sources: EU EUDAMED, US FDA

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    ATRAUMATIC VASCULAR CLAMPS

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GEN4 DIGITAL

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828112673·GEN4 DIGITAL

    GEN4 DIGITAL

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828109635·GEN4 DIGITAL

    GEN4 DIGITAL

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828111669·GEN4 DIGITAL

    GEN4 DIGITAL

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828111577·GEN4 DIGITAL

    GEN4 DIGITAL

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828111775·GEN4 DIGITAL

    KETAC-CEM IN REF. TO K802048

    FDA 510(k)
    FDA Class 2 ·Dental

    Kyocera Medical Technologies, Inc.

    FDA UDI
    KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523166015·MIS Acetabular Reamer, 48mm

    JBC OPAQUE AND GLITTER

    FDA 510(k)
    FDA Class 2 ·Dental

    POWDER FREE NEOPRENE EXAMINATION GLOVES, NON STERILE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    GLIDESHEATH SLENDER NITINOL (CONVENIENCE KIT)

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code DYB·February 21, 2018

    NORIAN REINFORCED FAST SET PUTTY/3CC

    FDA Adverse Event
    Malfunction ·SYNTHES SELZACH·Product code GXP·May 19, 2015

    PAINSMART IOD

    FDA Adverse Event
    Malfunction ·MOOG DEVICE GROUP·Product code FRN·April 22, 2013

    TANDEM T:SLIM INSULIN DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE INC.·Product code LZG·September 15, 2014

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 18, 2011

    GLIDESHEATH SLENDER NITINOL (CONVENIENCE KIT)

    FDA Adverse Event
    Malfunction ·TERUMO MEDICAL CORPORATION·Product code DYB·December 16, 2019

    VICRYL PLUS POLYGLACTIN 910 SUTURE UNKNOWN PROD

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAM·June 4, 2025

    UNK - SCREWS: LOCKING

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HWC·December 30, 2022

    UNK - PLATES: 3.5/4.5 MM LCP METAPHYSEAL PLATE

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HWC·December 30, 2022

    Baylis Medical TorFlex Transseptal Guiding Sheath, Rx Only, non-pyrogenic, sterile. Product Usage: The TorFlex Transseptal Guiding Sheath kit (K102948) is a single use device consisting of three components: a sheath, a dilator, and a J-tipped guidewire. The kit is designed for safe and easy catheterization and angiography of specific heart chambers and locations.

    FDA Recall
    Terminated ·Baylis Medical Corp 5959 TransCanada Highway Montreal Canada·Product code DYB·September 23, 2013