BEUDAMED
    34 results · 22ms · 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.

    LINA GOLD LOOP HC

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    NexxZr™ T / D-100-14-NT-C400-SD

    FDA UDI
    SAGEMAX BIOCERAMICS, INC·00842271113450·

    PARKHOUSE NEEDLE HOLDER

    FDA UDI
    SONTEC INSTRUMENTS, INC.·00192896089969·PARKHOUSE NEEDLE HOLDER TUNGSTEN CARBIDE SERRAT...

    Reef TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981190552·Interbody, 11mm x 32mm x 13mm, 15 Deg

    WaveForm TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981288860·Interbody, 11mm x 32mm x 13mm, 15 Deg, 3D

    Reef TH

    FDA UDI
    Seaspine Orthopedics Corporation·10889981200855·Interbody, 11mm x 32mm x 13mm, 15 deg

    Reef TO

    FDA UDI
    Seaspine Orthopedics Corporation·10889981204709·Trial, 11mm x 32mm x 13mm, 15 Deg

    Reef TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981192860·Interbody, 11mm x 32mm x 13mm, 15 deg

    Reef TA

    FDA UDI
    Seaspine Orthopedics Corporation·10889981207977·Trial, 11mm x 32mm x 13mm, 15 deg

    SITE-RITE IV ULTRASOUND SYSTEM

    FDA 510(k)
    FDA Class 2 ·Radiology

    VECTOR EVENT GRID ARCHITECTURE (VEGA) SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VERSAPOINT

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code JOS·January 5, 2005

    VERSAPOINT

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code JOS·January 5, 2005

    VERSAPOINT

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code JOS·January 5, 2005

    VERSAPOINT

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code JOS·January 5, 2005

    VERSAPOINT

    FDA Adverse Event
    Malfunction ·ETHICON, INC.·Product code JOS·January 5, 2005

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·September 28, 2023

    DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·August 29, 2019

    INTREL 3

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., MED REL·Product code LGW·August 2, 2011

    SURESTEP

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code CGA·September 10, 1999