BEUDAMED
    26 results · 22ms · Sources: EU EUDAMED, US FDA

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    DC-30/DC-32/DC-28/DC-26/DC-25/DC-20/DC-30 Exp/DC-32 Exp Diagnostic Ultrasound System

    FDA 510(k)
    FDA Class 2 ·Radiology

    Blade Handle

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112366·CHUCK HANDLE #3K 10CM LONG

    Blade Handle

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112373·CHUCK HANDLE #3KA 7.5CM LONG

    Blade Handle

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112380·BARD-PARKER HANDLE #3

    GALT MEDICAL GUIDEWIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEPILASE YAGLASE ND:YAG LASER SYSTEM AND ACCESSORIES

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

    UNK

    FDA Adverse Event
    Injury ·HOWMEDICA INC.·Product code JWH·February 23, 1999

    BIOCELL GEL-FILLED MAMMARY

    FDA Adverse Event
    Injury ·MCGHAN MEDICAL CORP.·Product code FTR·December 30, 1998

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·October 17, 2014

    BARD POWERPORT

    FDA Adverse Event
    Injury ·CR BARD·Product code LJT·August 5, 2011

    PRECISION®

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 2, 2013

    XP-XP Tibial Tray - Interlok 87 mm Item # 195760

    FDA Enforcement
    Class II ·Terminated·Zimmer Biomet, Inc.·September 18, 2019

    HANDPIECE MICS

    FDA Adverse Event
    Malfunction ·MAKO SURGICAL CORP.·Product code OLO·February 12, 2018

    CONTOUR CURVED CUTTER STAPLER

    FDA Adverse Event
    Injury ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·April 15, 2020

    STANDARD CUFF

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL PUERTO RICO, INC.·Product code LWQ·April 2, 1998

    MUSTANG

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·August 26, 2020

    ELUVIATM DRUG-ELUTING VASCULAR STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NIU·August 26, 2020

    ELUVIATM DRUG-ELUTING VASCULAR STENT SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NIU·August 26, 2020

    SILK SUTURE UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code GAP·November 1, 2022

    INTELLANAV MIFI OPEN-IRRIGATED ABLATION CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code OAD·February 25, 2021