BEUDAMED
    15 results · 19ms · Sources: EU EUDAMED, US FDA

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    JBAIDS ANTHRAX DETECTION KIT

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Corneal Scissor

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896102545·Scheie-Westcott Corneal Section Scissors Right

    VENFLON 2 PNK 20GA IV CANNULA

    FDA Adverse Event
    Malfunction ·Product code FOZ·September 13, 2021

    MEMOMETAL NAVIS BONE PLATING SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HIGH SPEED EMG MODULE

    FDA 510(k)
    FDA Class 2 ·Neurology

    PROMUS ELEMENT? PLUS

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·May 29, 2013

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 16, 2011

    DEXTRUS 4137

    FDA Adverse Event
    Injury ·BIOTRONIK GMBH AND CO.·Product code DTB·August 21, 2008

    ROD, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·May 9, 2019

    PEDICLE SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·May 9, 2019

    PEDICLE SCREW, UNKNOWN SIZE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET SPINE INC.·Product code NKB·May 9, 2019

    BAKRI TAMPONADE BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code KNA·January 10, 2018

    Kimberly Clark Microcuff Endotracheal Tube, Pediatric Oral Curved, sizes 3.0mm, 3.5mm, 4.0mm and 4.5mm, Rx Only, Sterile, Manufacturer: Kimberly-Clark NV Belgicastraat 13, 1930 Zaventem, Belgium, Made in Malaysia

    FDA Recall
    Terminated ·Kimberly-Clark Corporation·Product code BTR·June 4, 2007

    Kimberly-Clark Microcuff Endotracheal Tube, Pediatric Oral/Nasal Magill, sizes 3.0mm, 3.5mm, 4.0mm, and 4.5mm, Rx Only, Sterile, Manufacturer: Kimberly-Clark NV Belgicastraat 13, 1930 Zaventem, Belgium, Made in Malaysia

    FDA Recall
    Terminated ·Kimberly-Clark Corporation·Product code BTR·June 4, 2007

    BIOMET StageOne Knee Tibial Cement Spacer Mold, 75 MM, Silicone, Sterile, Item 433175.

    FDA Enforcement
    Class II ·Terminated·Biomet, Inc.·April 15, 2020