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

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    PARCUS DRAW TIGHT 1.8MM SINGLE-LOADED SUTURE ANCHOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04049772814565·GENUMEDI SAND SIZE V

    ArgenZ HT+ 95x25 D4

    FDA UDI
    ARGEN CORPORATION, THE·D818122805·Dental porcelain/ceramic restoration kit

    PROTEUS PTA BALLOON CATHETER WITH EMBOLIC CAPTURE FEATURE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    KIMGUARD ONE-STEP STERILIZATION WRAP

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CLS SPOTORNO, EXPANSION SHELL, UNCEMENTED, ø 58

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·February 5, 2025

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 21, 2013

    EXTENSION SET

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·June 14, 2011

    COAGUCHEK S SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JPA·August 14, 2008

    PEN NDL 31GA 5MM 100 BX 1200 LA

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·July 1, 2020

    MANTIS REDUX BLOCKER

    FDA Adverse Event
    Malfunction ·STRYKER SPINE-US·Product code NKB·November 27, 2019

    CLS EXPANSION CUP 48 MM

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·February 25, 2019

    Depuy P.F.C. E knee system, TC3 tibial insert; polyethylene tibial insert, Sz 4, 20.0 mm; Ref 96-0544.

    FDA Recall
    Terminated ·Depuy Orthopaedics, Inc.·Product code NJL·May 26, 2005