BEUDAMED
    891 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.
    Filters Regulation: Us FDA ×

    MEDRAD Imaging Bulk Package Transfer Spike

    FDA UDI
    Bayer Medical Care Inc.·00616258022369·ASSY,IBP TRANSFER SPIKE,FINAL (86613735)

    Titan Reverse Shoulder System

    FDA UDI
    Smith & Nephew, Inc.·00885556863732·REVERSE BASEPLATE 25MM

    AETOS Shoulder System

    FDA UDI
    Smith & Nephew, Inc.·00885556808436·GLENOID BASEPLATE CENTERED

    AETOS Shoulder System

    FDA UDI
    Smith & Nephew, Inc.·00885556814383·10 DEG AUGMENT BASEPLATE FULL WEDGE

    AETOS Shoulder System

    FDA UDI
    Smith & Nephew, Inc.·00885556808443·GLENOID BASEPLATE ECCENTRIC

    AETOS Shoulder System

    FDA UDI
    Smith & Nephew, Inc.·00885556814390·15 DEG AUGMENT BASEPLATE FULL WEDGE

    Titan Reverse Shoulder System

    FDA UDI
    Smith & Nephew, Inc.·00885556860281·RSS GLENOID BASEPLATE-S

    Titan Reverse Shoulder System

    FDA UDI
    Smith & Nephew, Inc.·00885556863725·REVERSE BASEPLATE 15MM

    Titan™

    FDA UDI
    Ascension Orthopedics, Inc.·10381780467656·RSS Glenoid Baseplate-S

    Buttress

    FDA UDI
    Genesys Orthopedics Systems LLC·M719GBP2220·Dual Screw Buttress Plate

    SURGASSIST CIRCULAR STAPLER 21MM DLU

    FDA Adverse Event
    Malfunction ·POWER MEDICAL INTERVENTIONS·Product code GDW·June 15, 2005

    Titan™ Reverse Shoulder System

    FDA UDI
    Ascension Orthopedics, Inc.·10381780121688·The Titan Reverse Shoulder baseplate is a gleno...

    Titan™ Reverse Shoulder System

    FDA UDI
    Ascension Orthopedics, Inc.·10381780121695·The Titan Reverse Shoulder baseplate is a gleno...

    ECHELON FLEX 45 COMPACT

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·September 18, 2024

    PROLENE MESH 3INX6IN

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code FTL·May 8, 2022

    POWERED 60 ECHELON +, 340MM SHAFT

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·March 1, 2023

    ETHILON NON ABS SUR SUT USP 4-0 70CM

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAR·March 25, 2022

    ETHILON 2-0 45MM 70CM

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAR·March 25, 2022

    ETHILON 2-0 45MM 70CM

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAR·March 28, 2022

    MALLA PROLENE 15CM X 15CM

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code FTL·May 8, 2022