Documenten - Waarschuwingen van fabrikanten medische hulpmiddelen
538 publicaties over Waarschuwingen van fabrikanten medische hulpmiddelen
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Uptake Medical Technology 12July2019 - InterVapor System
Patiënten met bloedingsstoornissen, patiënten die antistollingstherapie ondergaan en patiënten met instabiele cardiovasculaire ...
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SHENZHEN MINDRAY CP1812-JH00380 - BeneHeart D1
Het potentiële probleem kan worden veroorzaakt door de interne draad naar de defibrillatoraansluiting die wordt gebruikt op de ...
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MESI 05_07_2019 - Automated Ankle-Brachial Index measuring device (MESI ABPI MD)
After recently performed calibrations of the ABPI MD, our UK distributor noticed that the cuffs are overinflating. This does not ...
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Edwards Lifesciences FCA-140 - Edwards CENTERA transkatheter-hartklepsysteem
Edwards heeft meldingen ontvangen van problemen bij het volgen en manipuleren van het CENTERA-systeem rond de aortaboog, die ...
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Leonhard Lang CAP-19-0115 - Mindray- and Weinmann Defibrillation Electrodes
Fault: Electrode material may be trapped between the eyelet of the cable and the rivet in the affected electrodes. Potential ...
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GE Healthcare Finland Oy - FMI 39001 - ECG trunk cables, ECG Leadwires
ECG trunk cables and leadwires may reduce the amount of energy reaching the patient during defibrillation, potentially limiting ...
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Teleflex Medical - EIF-000362 - Arterial Catheterization Set
Arrow International is voluntarily issuing a Field Safety Notice for these products as they may contain the incorrect IFU, which ...
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Maquet_Getinge 2249723-05_17_2019-001-C - Datascope Intra-Aortic Balloon Pumps (IABP)
This field correction is being conducted to ensure that all IABP users follow each device's Operating Instructions Manual for ...
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Philips, FSCA 86100188A-IR, HeartStart MRx Defibrillator/Monitor
Philips heeft vastgesteld dat de M3539A netvoedingsmodule voor de HeartStart MRxmonitor/defibrillator mogelijk sneller defect kan ...
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Aesculap AG, FSCA 235, Synthetic vascular graft
In the cause of an internal investigation Aesculap AG became aware of a product counterfeit of the UNI Graft K DV vascular ...