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Documenten - Waarschuwingen van fabrikanten medische hulpmiddelen

53 publicaties over Waarschuwingen van fabrikanten medische hulpmiddelen

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  1. Acandis GmbH FSCA 22-001 - DERIVO® 2 Embolisation Device

    We have received an increasing number of complaints from customers who have reported difficulty in delivery of devices through ...

    Waarschuwing | 26-01-2022

  2. Technomed Europe CAPA 21-009_NCR 21-081 - Disposable Subdermal Needle Electrode, corkscrew

    Technomed is issuing a Medical Device Recall notice following the observation of a high risk that the needle electrode could ...

    Waarschuwing | 23-12-2021

  3. Medtronic, Inc., FSN-FA948, ARESTM Antibiotic-Impregnated Catheter

    Medtronic roept vrijwillig specifieke partijen ARES™ met antibiotica geïmpregneerde shuntkatheters terug.

    Waarschuwing | 10-12-2020

  4. Aesculap AG, FSN-FSCA249, AESCULAP AEOS

    With this letter Aesculap AG would like to inform you about a potential malfunction of product Aesculap Aeos®.

    Waarschuwing | 20-10-2020

  5. Medtronic FA933 - InterStim Percutaneous Extension Connector

    Middels deze brief willen we u op de hoogte stellen van het mogelijk verschuiven van de percutane extensieconnector tijdens een ...

    Waarschuwing | 15-10-2020

  6. Integra LifeSciences Production Corporation, FSN-N-2020-HHE-014, CODMAN® BACTISEAL® EVD CATHETER SET

    The purpose of this letter is to notify you that the legal manufacturer Integra LifeSciences, is voluntarily issuing a Field ...

    Waarschuwing | 08-10-2020

  7. Micro Therapeutics Inc. DBA ev3 Neurovascular, FSN-FA929, PipelineTM Flex Embolization Device (with Shield TechnologyTM)

    Medtronic is providing this notice regarding a labeling update to ensure awareness among Pipeline™ Flex and Pipeline™ Flex with ...

    Waarschuwing | 02-09-2020

  8. The Magstim Company Ltd, FSN-FCA-2020-02, Neurosign V4

    Magstim are issuing a voluntary corrective action following reports that manipulation of the cable which connects the ...

    Waarschuwing | 01-07-2020

  9. Elekta Instrument AB, FCA-EIAB-0008, Leksell Vantage Arc System

    Elekta has found that the design of the Instrument Carrier is not optimal which may cause the locking mechanism at the interface ...

    Waarschuwing | 08-06-2020

  10. Medtronic Inc FA912 Verify Therapy App

    This letter is to notify you of the correction of an inadvertent automatic update to Model A511 Clinician Therapy Application ...

    Waarschuwing | 22-04-2020

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