BEUDAMED
    11 results · 24ms · Sources: EU EUDAMED, US FDA

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    Marco Ultra M3, Marco Ultra M4

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    OSSEOTITE, OSSEOTITE NY, CERTAIN, CERTAIN NT, PREVAIL, CERTAIN PREVAIL, XP, MICROMINIPLANT, DENTAL IMPLANTS

    FDA 510(k)
    FDA Class 2 ·Dental

    ZENITH PEDICLE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    TIBIAL INSERT FIXED SPHERE FLEX SIZE 4/14 MM R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·March 16, 2018

    PRADO™ Lumbar Interbody Fusion System

    FDA UDI
    Pt. Solutions, LLC·G616RAFS162636060·NON-STERILE PLANAR, PRADO A SYMMETRIC PEEK IBFD...

    PRADO™ Lumbar Interbody Fusion System

    FDA UDI
    Pt. Solutions, LLC·G616RAFS162636110·NON-STERILE PLANAR, PRADO A ASYMMETRIC PEEK IBF...

    PRADO™ Lumbar Interbody Fusion System

    FDA UDI
    Pt. Solutions, LLC·G616RAFS162636120·NON-STERILE PLANAR, PRADO A SYMMETRIC PEEK IBFD...

    S-ROM*SLEEVE PRX ZTT, 18D-LRG

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code LPH·September 23, 2022

    CAPSURE SENSE

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·October 10, 2014

    COAGUCHEK ® XS SYSTEM

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code GJS·June 11, 2013

    ADVANCE(R) II TIBIAL BASE

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code HRY·October 20, 2015