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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    nva, nvp, and nvt

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Sklar®

    FDA UDI
    SKLAR CORPORATION·10649111119927·LEXER SCISS STR 6 1/4" TC

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172971369·

    UniTip Catheter

    FDA UDI
    Unisensor AG·07640172973233·

    CARESCAPE MODEL V100 VITAL SIGNS MONITOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    DEPUY PINNACLE METAL-ON-METAL ACETABULAR CUP LINERS

    FDA 510(k)
    FDA Class 3 ·Orthopedic

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·July 14, 2011

    MAX PRI DCM TIB BRNG12X71/75MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JWH·June 11, 2013

    ATTAIN ABILITY

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

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code HSD·January 9, 2024

    SCREWDRIVER BIT T15, AO FITTING

    FDA Adverse Event
    Malfunction ·STRYKER GMBH·Product code HWC·October 6, 2017

    SCREWDRIVER BIT T15, AO FITTING

    FDA Adverse Event
    Malfunction ·STRYKER GMBH·Product code HWC·October 6, 2017

    EQUINOXE PRESERVE STEM 12MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·May 29, 2019

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·July 2, 2019

    EQUINOXE REVERSE 46MM GLENOSPHERE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·October 2, 2024