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

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    HEATED RESPIRATORY HUMIDIFIER HC100

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Damon 3

    FDA UDI
    ORMCO CORPORATION·00889989052756·L3R DAMON 3 .022 +7/+5/0 HK

    STERILE DISPOSABLE DRAPE/OPHTHALMIC SURGERY

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

    .010 HI-TORQUE GUIDE WIRES WITH PRESHAPED TIP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PADGETT MODEL S SLIMLINE ELECTRIC DERMATOME

    FDA Adverse Event
    Malfunction ·INTEGRA LIFESCIENCES CORPORATION OH/USA·Product code GFD·May 14, 2015

    SYS 2000 FOOTSWITCH

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORPORATION·Product code GEI·June 5, 2014

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC·Product code GJS·January 10, 2013

    EON MINI IPG

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·November 4, 2010

    REGENEREX PRIMARY PATELLA SERIES A ¿ 3 PEG 34MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code MBH·November 8, 2016

    SERIES A PAT STD 31 3 PEG

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·May 9, 2023

    BIOMET CC CRUCIATE TRAY 67MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·May 9, 2023

    VANGUARD CR ILOK FEM-LT 62.5

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·May 9, 2023

    BIOMET StageOne Knee Femoral Cement Spacer Mold, 65 MM, Silicone, Sterile, Item 432165.

    FDA Enforcement
    Class II ·Terminated·Biomet, Inc.·April 15, 2020