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

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    Ophthalmic Knife

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113332·PHACO KNIFE 3.0MM ANGLED (BX/5)

    Fingertip Pulse Oximeter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517578334·CoRoent Ant TLIF Ti, 10x12x32mm 4°

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·07613327682724·Pediatr. mandib. distractor 25mm left

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707037163·DB BRACKETS SING 22 CUS

    NORMED TITANIUM CALCANEUS PLATING WITH LOCKING SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODIFIED TO MODULAR FR SEVERE BONE LOSS TRAUMA

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NOBELACTIVE TIULTRA NP 3.5X13MM

    FDA Adverse Event
    Injury ·NOBEL BIOCARE AB·Product code DZE·May 31, 2021

    NOBELACTIVE TIULTRA NP 3.5X13MM

    FDA Adverse Event
    Injury ·NOBEL BIOCARE AB·Product code DZE·May 31, 2021

    REVANESSE VERSA+ 1.2 ML

    FDA Adverse Event
    Injury ·PROLLENIUM MEDICAL TECHNOLOGIES INC·Product code LMH·June 12, 2023

    SPECTRUM IQ INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·June 14, 2023

    ATTUNE PS FB INSRT SZ 6 12MM

    FDA Adverse Event
    Malfunction ·DEPUY IRELAND - 9616671·Product code JWH·September 6, 2023

    PENUMBRA SYSTEM RED 62 REPERFUSION CATHETER

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·May 26, 2023

    SPECTRUM IQ INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·June 14, 2023

    INTERA 3000

    FDA Adverse Event
    Malfunction ·INTERA ONCOLOGY·Product code LKK·December 6, 2023

    RESPIRONICS

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code MNT·October 19, 2023

    OSI

    FDA Adverse Event
    Injury ·MIZUHOSI·Product code FQO·October 16, 2008

    EZ BREATHE ATOMIZER

    FDA Adverse Event
    HEALTH & LIFE (SUZHOU) CO., LTD.·Product code CCQ·June 25, 2013

    POLYURETHANE, FLEXIBLE BRAIDED TUBING

    FDA Adverse Event
    Malfunction ·MERIT MEDICAL SYSTEMS, INC.·Product code DXJ·August 5, 2011

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code NKB·October 27, 2020