BEUDAMED
    181 results · 38ms · Sources: EU EUDAMED, US FDA

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    3Delta Crown

    FDA 510(k)
    FDA Class 2 ·Dental

    n.a.

    FDA UDI
    Karl Storz GmbH & Co. KG·04048551072646·Elevator with Scalpel Handle No.7

    Sochi

    FDA UDI
    Altus Spine, LLC·00843210167237·Offset Hook, Left, Small

    ALEUTIAN Interbody Systems

    FDA UDI
    VB Spine LLC·10888857557475·Removal Tool Size 7 x 305 mm

    Atoll™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981052898·Offset Hook (left) - small. The Atoll OCT Spina...

    INTELLISPACE PACS 4.X

    FDA 510(k)
    FDA Class 2 ·Radiology

    CAPIOX ARTERIAL FILTER WITH X-COATING, PRODUCT CODE CX*AFO2X

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Coral

    FDA UDI
    Seaspine Orthopedics Corporation·10889981027834·Offset Hook Right - Small. The Coral Spinal Sys...

    Stainless Steel

    FDA UDI
    Seaspine Orthopedics Corporation·10889981028503·Offset Hook Right Small. The Stainless Steel Sp...

    Coral

    FDA UDI
    Seaspine Orthopedics Corporation·10889981027827·Offset Hook Left - Small. The Coral Spinal Syst...

    Stainless Steel

    FDA UDI
    Seaspine Orthopedics Corporation·10889981028497·Offset Hook Left Small. The Stainless Steel Spi...

    BEBACK CROSSING CATHETER

    FDA Adverse Event
    Malfunction ·BENTLEY INNOMED GMBH·Product code PDU·December 23, 2025

    GMK TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·October 22, 2025

    GÜNTHER TULIP VENA CAVA FILTER JUGULAR APPROACH

    FDA Adverse Event
    Malfunction ·WILLIAM COOK EUROPE·Product code DTK·July 12, 2022

    BEBACK CROSSING CATHETER

    FDA Adverse Event
    Malfunction ·BENTLEY INNOMED GMBH·Product code PDU·November 21, 2025

    BEBACK CROSSING CATHETER

    FDA Adverse Event
    Malfunction ·BENTLEY INNOMED GMBH·Product code PDU·April 30, 2025

    BEBACK CROSSING CATHETER

    FDA Adverse Event
    Malfunction ·BENTLEY INNOMED GMBH·Product code PDU·March 6, 2025

    AMK CONGR PS INS SIZE 4 14MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·August 10, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·October 29, 2014

    DEXTRUS MED ACCESS RETRACTOR

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GCJ·July 8, 2013