BEUDAMED
    46 results · 21ms · Sources: EU EUDAMED, US FDA

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    ICONACY(TM) I-Hip (TM)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    POUR-PLUS

    FDA UDI
    Denplus Inc·D8451151307·POUR-PLUS, MDP, 11.3 kg

    MEDI

    FDA UDI
    MEDI MANUFACTURING, INC.·04064984699595·GENUMEDI PSS BLUE, SIZE VII

    HHM

    FDA UDI
    Oticon A/S·05707131288738·H110V2, DESIGNRITE 10 WL THP HHM

    Echo FX™ Hip System

    FDA UDI
    Biomet Orthopedics, LLC·00887868261084·

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111139567·DOYEN SCISS 7" STR B/B

    ECHO FX HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304467910·

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575288892·Orthopaedic implant aiming/guiding block, reusa...

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575288922·Body femoral/tibial extension stem, uncoated - ...

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575288908·Orthopaedic implant aiming/guiding block, reusa...

    Endo-Model Knee System - Instruments

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575289028·Body femoral/tibial extension stem, uncoated - ...

    BLOOD GLUCOSE MONITORING SYSTEM, MODELS AG-6081 AND AG-6951

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    SYNCHRON SYSTEMS BEBZODIAZAPINE (EBNZ) REAGENT

    FDA 510(k)
    FDA Class 2 ·Clinical Toxicology

    BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B LABORATORY KIT

    FDA Adverse Event
    Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·March 3, 2026

    G7 LONGEVITY HIGH WALL 40MM F

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code LPH·May 18, 2022

    PALACOS

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LOD·February 16, 2018

    2.7MM/3.5MM VA-LCP EXT MEDL DSTL HUM PL 4H/LT/111MM-LONG

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·June 7, 2013

    LCS COMPLETE FEM POR L STD+

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code MBH·June 30, 2011

    ROTALINK CATHETER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC·Product code MCX·September 4, 2008

    PALACOS

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LOD·February 16, 2018