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

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    MICROINFERTILITY FORCEPS, TITANIUM

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

    TREONIC C30

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CHERMEL OSTEOTOMES

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    DIGNISHIELD STOOL MANAGEMENT SYSTEM

    FDA Adverse Event
    Malfunction ·C. R. BARD, INC.·Product code KNT·April 26, 2024

    PORT ACCESS NEEDLE

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS, INC.·Product code FPA·April 22, 2024

    VERSACARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·March 12, 2014

    LIFEVEST WCD 3000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·November 2, 2012

    STENOSCOPE

    FDA Adverse Event
    Malfunction ·GE MED SYSTEMS (INDIA) PRIVATE LTD (GE PRIVATE)·Product code JAA·September 23, 2010

    Magic3 Go Intermittent Urinary Catheters, pediatric Catalog Numbers: a) REF 52810G

    FDA Recall
    Open, Classified ·C.R. Bard Inc·Product code EZD·April 20, 2023

    X-Stream Irrigation System (Catalog No. 5551000) and X-Stream Irrigation System Refurbished (Catalog No. 9551000)

    FDA Recall
    Open, Classified ·Davol, Inc.·Product code GCJ·June 27, 2022

    Magic3 Go Intermittent Urinary Catheters, Female Catalog Numbers: a) REF 51808, b) REF 51810, c) REF 51812, d) REF 51814, e) REF 51816, f) REF 51818

    FDA Recall
    Open, Classified ·C.R. Bard Inc·Product code EZD·April 20, 2023

    HydroSil Go Intermittent Urinary Catheters, Catalog Numbers: a) REF 71808, b) REF 71810, c) REF 71812, d) REF 71814, e) REF 71816, f) REF 71818

    FDA Recall
    Open, Classified ·C.R. Bard Inc·Product code EZD·April 20, 2023

    BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382903949106 BD Connecta" Stopcocks are used to administer fluids or medication through one or two different ports via an IV cannula or extension tube. The ports can be used to sample blood or for hemodynamic monitoring. When used with IV lipid nutritional products, the stopcock device can be used for up to 24 hours.

    FDA Recall
    Open, Classified ·Product code FMG·May 21, 2026

    Medivance Neonatal ArcticGel Pads, REF: 31802, 3180202, 31802C

    FDA Recall
    Open, Classified ·Medivance Inc.·Product code DWJ·February 16, 2024

    BD SARS-CoV-2 Reagents for BD MAX" Systems. RT-PCR test to detect SARS-CoV-2 in nasal, nasopharyngeal, oropharyngeal swab specimens, and saliva specimens.

    FDA Recall
    Open, Classified ·Becton Dickinson & Co.·Product code QJR·May 7, 2024

    Magic3 Go Intermittent Urinary Catheters, male Catalog Numbers: a) REF 50810G, b) REF 50812G, c) REF 50814G, d) REF 50816G, e) REF 50818G, f) REF 53810G, g) REF 53812G, h) REF 53814G, i) REF 53816G, j) REF 53818G, k) REF 53820G

    FDA Recall
    Open, Classified ·C.R. Bard Inc·Product code EZD·April 20, 2023

    Snowden-Pencer MIS DIAMOND-TOUCH CLAMP DEBAKEY 35 MM JAW 5MM, 32CM, RATCHETED, REF SP90-7044; endoscopic surgical device

    FDA Recall
    Open, Classified ·Carefusion 2200 Inc 75 N Fairway Dr Vernon Hills IL 60061-1845·Product code GCJ·July 13, 2023

    BD Recanalization System, REF: BDRECANSYSTEM

    FDA Recall
    Open, Classified ·Bard Peripheral Vascular Inc·Product code PDU·November 14, 2023

    CD11b APC: ASR, REF: 340936, and CE, REF: 333143

    FDA Recall
    Open, Classified ·Becton, Dickinson and Company, BD Biosciences·Product code MVU·October 25, 2023

    Snowden-Pencer MIS DIAMOND-TOUCH DISSECTOR DIAMOND JAW 5MM, 32CM, RATCHETED, REF SP90-7071; endoscopic surgical device

    FDA Recall
    Open, Classified ·Carefusion 2200 Inc 75 N Fairway Dr Vernon Hills IL 60061-1845·Product code GCJ·July 13, 2023