Documenten - Waarschuwingen van fabrikanten medische hulpmiddelen
437 publicaties over Waarschuwingen van fabrikanten medische hulpmiddelen
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Merit Medical Systems, 1721504-08.23.24-008R, Monarch Inflation
Merit Medical Systems, Inc. is voluntarily conducting a recall of specific lots of MONARCH® Inflation Devices due to a packaging ...
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Maquet Cardiopulmonary GmbH, 997581, Cardiohelp-i
During service measurements in course of Field Action 881841 on the CARDIOHELP-i devices in the field, it was identified that the ...
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Maquet Cardiopulmonary GmbH, 782698, BS 3/8x3/32 L1.7
Since a label change in 2021, a label template with a Unique Device Identifier (UDI) was used for the type label attached to the ...
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B. Braun Melsungen, RECALL 2019-03-07 AS/LS, Certofix® Quattro
Omdat het defect niet kan worden beperkt, moet het hele Certofix Quattro-productaanbod worden teruggeroepen.
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SCHILLER AG, SAGQI-874, Tempus LS
SCHILLER AG heeft ontbrekende informatie achterhaald in de gebruiksaanwijzing van de Tempus LS. De informatie die ontbrak, was ...
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B.Braun Melsungen AG, FSCA-2023-08-21, Original Perfusor® Line
Tijdens onze post-market surveillance-activiteiten hebben we het risico vastgesteld dat luer-connectoren loskomen van de ...
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Draeger Medical Systems, Inc., PR142097, Infinity Acute Care System .M540.
Draeger Medical Systems, Inc. (DMSI) has become aware during testing in conjunction with our global market surveillance ...
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Remote Diagnostic, FA-009, Tempus Pro
Samenvatting: In de brief staat dat we een intermitterende softwarefout hebben ontdekt als onderdeel van een interne ...
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Remote Diagnostic Technologies Ltd., Tempus Pro
An issue has been identified with the Tempus Pro Monitor where an error may occur during video laryngoscope use with the Tempus ...
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Remote Diagnostic Technologies Ltd., 2023-CC-EC-005-IR, Tempus Pro
An issue has been identified with the Tempus Pro Monitor where an error may occur during video laryngoscope use with the Tempus ...