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

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    DENLASER, MODEL 800

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    CAMLOG® Screw-Line-compatible

    FDA UDI
    Preat Corporation·00842092181485·Titanium Scan Body for CAMLOG® Screw-Line-compa...

    CRITI-KIT 200 EMERGENCY MEDICAL KIT

    FDA UDI
    HF ACQUISITION CO. LLC·00850065007403·

    SILK NONABSORBABLE SURGICAL SUTURES, USP

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MINICAM

    FDA 510(k)
    FDA Class 1 ·Dental

    AUTOSOFT XC

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 13, 2024

    INSET

    FDA Adverse Event
    Injury ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·September 9, 2025

    INSET

    FDA Adverse Event
    Injury ·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·September 9, 2025

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·February 7, 2013

    SYNCHROMED II 8637-40

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code LKK·February 22, 2011

    OASYS BRAND CONTACT LENSES WITH HYDRACLEAR

    FDA Adverse Event
    Injury ·VISTAKON·Product code LPL·February 26, 2008

    ARTICULAR SURFACE FIXED BEARING CRUCIATE RETAINING (CR)

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·March 9, 2023

    UNKNOWN OXFORD TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·August 4, 2020

    UNKNOWN OXFORD BEARING

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JWH·August 4, 2020

    UNK OXFORD TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code HRY·August 24, 2021

    UNK OXFORD FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·August 24, 2021

    ZIMMER SKIN GRAFT MESHER

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL, INC.·Product code FZW·April 10, 2023

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·March 29, 2023

    VITEK® 2 AST-GP75 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·December 12, 2018

    VITEK® 2 AST-GP75 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC.·Product code LON·December 12, 2018