BEUDAMED
    10,000 results · 28ms · 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 ×

    OptiMap™ Fiber Optic Cable

    FDA UDI
    Cortex, Inc.·00850064686104·OptiMap™ Fiber Optic Cable

    Millennium

    FDA UDI
    Avalign Technologies, Inc.·00190776192310·ST MARKS DEEP PELVIC RETR WDOYEN HANDLE

    CEMENT, BONE, VERTEBROPLASTY

    FDA Adverse Event
    Malfunction ·MEDTRONIC SPINE LLC.·Product code NDN·November 8, 2011

    MOMENTUM EL ICD DR

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LWS·June 11, 2024

    DAVINCI 5

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·March 5, 2026

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·July 9, 2025

    DAVINCI X

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·April 20, 2026

    RUSCH MRI COND FIBER OPTIC LARYN KIT

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code OGH·March 27, 2015

    AXIOM LUMINOS DRF

    FDA Adverse Event
    Injury ·SIEMENS HEALTHCARE GMBH·Product code OWB·December 30, 2021

    DAVINCI XI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·February 27, 2024

    FOCS BLADES, STANDARD HANDLE

    FDA Adverse Event
    Death ·RUSCH INC.·Product code EQN·March 16, 1999

    FOCS MACINTOSH 4 BLADE

    FDA Adverse Event
    Malfunction ·RUSCH INC.·Product code CAL·November 21, 2002

    BD CD5 PERCP-CY5.5 L17F12 ASR

    FDA Adverse Event
    Malfunction ·BD CARIBE, LTD·Product code MVU·July 21, 2022

    TRILOGY EVO

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·July 9, 2025

    SOMATOM SENSATION 64

    FDA Adverse Event
    Malfunction ·SIEMENS MEDICAL SOLUTIONS USA, INC.·Product code JAK·February 1, 2019

    DAVINCI XI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·November 3, 2025

    DAVINCI 5

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·March 10, 2026

    Cytomics FC 500 MPL with MXP software, Versions 2.0 & 2.1: Part #731419 KIT; FOC MXP 2.0 UPGRADE KIT; Part #731418 SWRE KIT; MXP 2.0 NEW USER; Part #772145 MXP 2.1 FOC Upgrade Kit; 771938 MXP 2.1 Software; Part #771952 FOC MXP 2.1 Upgrade Kit; Part #771953 New User MXP 2.1 Kit. The Cytomics FC 500 is a system for the qualitative and quantitative measurement of biological and physical properties of cells and other particles.

    FDA Recall
    Terminated ·Beckman Coulter Inc·Product code GKZ·August 29, 2006

    RUSCH FOCS ILS MACINTOSH BLADE

    FDA Adverse Event
    Malfunction ·TELEFLEX·Product code CCW·January 21, 2014

    FOCS OXIPORT FIBEROPTIC BLADE - MILLER

    FDA Adverse Event
    Malfunction ·RUSCH, INC.·Product code CAI·November 15, 2000