BEUDAMED
    23 results · 27ms · Sources: EU EUDAMED, US FDA

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    G210 InviCell Plus with SignipHy pH monitoring

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

    Phasix

    FDA UDI
    Davol Inc.·00801741107573·Phasix Mesh, 4" x 8" (10 cm x 20 cm), Rectangle

    Long Sheath Introducer

    FDA UDI
    ARGON MEDICAL DEVICES, INC.·00886333206889·7.5F Long Sheath Introducer

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694052191·2.0mm x 10 Degree ExtremiFuse Implant

    THINFLAP

    FDA UDI
    BIOMET MICROFIXATION, INC·00841036079826·

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M930719102010·Box Curette 10x20 ang.

    Life Instruments

    FDA UDI
    Life Instrument Corporation·M930719102000·Box Curette 10x20 str.

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694069984·ExtremiFuse 2mm 10 Degree Implant Sterile Qty 5

    BLUEPHASE 20I

    FDA 510(k)
    FDA Class 2 ·Dental

    ATRICURE DISSECTOR

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    NEEDLE 30GX1/2 IN FOR PHARM CUSTOMERS

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMI·April 16, 2021

    NEEDLE 30GX1/2 IN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMI·August 6, 2021

    SYRINGE 0.3ML 31G 6MM S/C U-100 RELION

    FDA Adverse Event
    Malfunction ·EMBECTA MEDICAL I LLC - HOLDREGE, NE·Product code FMF·June 9, 2025

    SYRINGE 0.3ML 31G 6MM S/C U-100 RELION

    FDA Adverse Event
    Malfunction ·EMBECTA MEDICAL I LLC - HOLDREGE, NE·Product code FMF·June 4, 2025

    SYRINGE 0.3ML 31G 6MM S/C U-100 RELION

    FDA Adverse Event
    Malfunction ·EMBECTA MEDICAL I LLC - HOLDREGE, NE·Product code FMF·June 4, 2025

    SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·October 21, 2014

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·June 21, 2013

    HOMECHOICE AUTOMATED PD SET WITH CASSETTE

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·August 4, 2011

    BD MICROLANCE¿ 3 HYPODERMIC NEEDLE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMI·March 17, 2023

    STERILE TRAC THINFLAP 18.5MM BENT BURR PLATE

    FDA Adverse Event
    Malfunction ·BIOMET MICROFIXATION·Product code JEY·May 16, 2018