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

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    ROTORBLADE SUTURE ANCHOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    artegral life

    FDA UDI
    Merz Dental GmbH·D7091993373·anteriors; shade C3; mould BIL

    Comprehensive® Reverse Shoulder

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LARYNGEAL SURFACE ELECTRODE

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    COMP RVRS 25MM BSPLT HA+ADPTR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·March 8, 2021

    NO 6. TRIATHLON TS PLUS TIBIAL INSERT X3 POLY 13MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JWH·March 7, 2013

    MINI KOMPRESSOR SCREW 18 MM

    FDA Adverse Event
    Other ·INEGRA LIFESCIENCES CORP. (INTEGRA-OHIO)·Product code HWC·February 8, 2011

    ATTAIN OTW

    FDA Adverse Event
    Injury ·MPRI·Product code LWP·August 8, 2014

    IMPACT Catheters, Balloon Dilatation and Esophageal Dilatation Catheter, Model Number 307, STERILE, Rx only --- Common/Usual Name: PTA and Esophageal Catheter --- Manufactured for: B. Braun Interventional Systems Inc., 824 Twelfth Avenue Bethlehem, PA18018 --- Manufactured by: NuMED, Inc. 2880 Main Street, Hopkinton, NY 12965 --- The Impact catheter is packaged in a straight sheath and then heat sealed in two Tyvek pouches. The inner pouch is the one that is deteriorating when exposed to the sunlight. The outer pouch retains its seal so the sterility is not compromised. --- 510 K931009 - Device Listing #D003206 and 510 K983373 - Device Listing # D003212, Class II device.

    FDA Recall
    Terminated ·Numed Inc·Product code LIT·September 23, 2009