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

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    HARDYDISK, PIPERACILLIN/TAZOBACTAM, 110MCG

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Henry Schein

    FDA UDI
    HENRY SCHEIN, INC.·00304040057742·Prophy Angle Snap On

    Custom Procedure Kit

    FDA UDI
    MEDIVATORS INC.·40677964002821·The ENDO CARRY-ON Procedure Kit contains all of...

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092117071·Zimmer TSV 4.5mm x 4.5mm Titanium Base

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810014602189·FHC BEACH CHAIR

    MINXRAY HF70D HIGH FREQUENCY PORTABLE DENTAL X-RAY UNIT

    FDA 510(k)
    FDA Class 2 ·Dental

    HARDYDISK, STREPTOMYCIN 10MCG

    FDA 510(k)
    FDA Class 2 ·Microbiology

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL UM-D·Product code FPA·January 3, 2025

    INTERSEAL IMPACTOR HOLE PLUG

    FDA Adverse Event
    WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LPH·July 23, 2010

    REVISION MODULAR STEM Ø20MM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code LZO·January 18, 2022

    55MM RIGHT STANDARD MANDIBULAR

    FDA Adverse Event
    BIOMET MICROFIXATION·Product code LZD·March 16, 2010

    8.0MM/4.0MM DRILL SLEEVE 164MM

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code FZX·March 12, 2013

    RESTORE ULTRA

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·February 17, 2011

    AED PLUS

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·February 14, 2008

    MiniArc Pro Single incision Sling System, Model number / Product Reference 9000261, Lot 936405xxx. Designed to treat female stress urinary incontinence.

    FDA Recall
    Terminated ·Astora·Product code PAH·October 26, 2015

    MiniArc Pro Single incision Sling System, Model number / Product Reference 9000261, Lot 936405xxx. Designed to treat female stress urinary incontinence.

    FDA Enforcement
    Class II ·Terminated·Astora·November 25, 2015

    Z.S.G.M. CUTTER 3:1 RATIO ( CAUTION: SHARP )

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL, INC.·Product code FZW·January 9, 2023

    1.5X4MM HT SD X-DR SCREW

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·February 5, 2016

    TRANSDERMAL CPS FAILSAFE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 2, 2018

    BIOLOX DELTA LNR 36MM 54-56MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·January 16, 2020