BEUDAMED
    68 results · 81ms · 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.

    Catheter Precision, Inc

    Manufacturer
    🇺🇸 United States·2 Basic UDI-DIs·2 Devices

    MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES

    Device
    EU MDR · Eu Md Class 1 ·Catheter Precision, Inc·On the market

    VIVO System

    Device
    EU MDR · Eu Md Class 1 ·Catheter Precision, Inc·On the market

    VIVO Positioning Patches

    FDA UDI
    Catheter Precision, Inc.·00851424007102·Patches are placed on the shoulder and sternum ...

    LockeT Suture Retention Device

    FDA UDI
    Catheter Precision, Inc.·00851424007140·LockeT is a safe and effective suture retention...

    VIVO

    FDA UDI
    Catheter Precision, Inc.·00851424007089·VIVO™ uses standard clinical inputs and proprie...

    DABRA Laser System

    FDA UDI
    Catheter Precision, Inc.·00842362100024·A mains electricity (AC-powered) Light Amplific...

    VIVO System

    FDA UDI
    Catheter Precision, Inc.·00851424007119·VIVO™ uses standard clinical inputs and proprie...

    DABRA 101 Catheter

    FDA UDI
    Catheter Precision, Inc.·00842362100031·Percutaneous Catheter

    Pharos

    FDA UDI
    Catheter Precision, Inc.·00842362100017·A mains electricity (AC-powered) Light Amplific...

    VIVO System

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·Catheter Precision, Inc·1 device

    VIVO Positioning Patches

    Basic UDI-DI
    EU MDR · Eu Md Class 1 ·Catheter Precision, Inc·1 device

    ACQMAP 3D IMAGING & MAPPING CATHETER

    FDA Adverse Event
    Injury ·ACUTUS MEDICAL, INC.·Product code MTD·January 19, 2021

    UNK_THERMOCOOL SF NAV

    FDA Adverse Event
    Death ·BIOSENSE WEBSTER INC·Product code LPB·June 9, 2022

    THERMOCOOL® SMART TOUCH® SF BI-DIRECTIONAL NAVIGATION CATHETER

    FDA Adverse Event
    Malfunction ·BIOSENSE WEBSTER INC·Product code LPB·March 26, 2023

    PRECISE SDS SELF EXPANDING

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code FGE·July 2, 2014

    PRECISE SDS SELF EXPANDING

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code FGE·July 2, 2014

    PERIFIX®

    FDA Adverse Event
    Malfunction ·B BRAUN MELSUNGEN AG·Product code OGE·September 26, 2024

    SHOCKWAVE IVL SYSTEM WITH THE SHOCKWAVE C2 CORONARY IVL CATHETER

    FDA Adverse Event
    Injury ·SHOCKWAVE MEDICAL, INC.·Product code QMG·October 4, 2023

    CARTO 3

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code DQK·June 13, 2017