Documenten - Waarschuwingen van fabrikanten medische hulpmiddelen
3.325 publicaties over Waarschuwingen van fabrikanten medische hulpmiddelen
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CareDx AB, A-2022-123, QTYPE 11
De mix in positieiop O21 in het O560-kanaal op de QTYPE-plaat is ontworpen om het DPB1*10: 01-allel te versterken, maar is gemeld ...
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Philips Medical Systems, FSCA 2021-CC-EC-012-IR, Infant.Child SMART Pads Cartridge, Adult SMART Pads Cartridge, Used with the HS1 Home and Onsite Defibrillators
Het is voorgekomen dat de gel van sommige elektroden die worden gebruikt voor de HS1/OnSite/Home-AED loskomt van de ...
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GENERI BIOTECH s.r.o., FSCA_UGT1A1_02_2022, gb PHARM UGT1A1
An incorrectly determined genotype may affect the confirmation or exclusion of Gilbert syndrome. Based on the genotype ...
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Datascope Corp. Getinge, 2249723-11.16.2022-001-C, Cardiosave Intra-Aortic Balloon Pumps
Datascope Corp., a subsidiary of Getinge, is initiating a voluntary Medical Device Correction for the Cardiosave Hybrid and ...
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Covidien llc, FA1286, Dermalon™ Monofilament Nylon sutures Monosof™ Monofilament Nylon sutures Novafil™
Medtronic heeft vastgesteld dat productiefouten in de verpakking van de genoemde niet-absorbeerbare hechtdraden een gat of rimpel ...
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EPOCAL Inc., POC 23-004, Epoc Host 2 and Epoc NXS Host
Siemens Healthcare Diagnostics Inc. has confirmed an issue through complaint investigation. The issue has the potential to affect ...
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Siemens Healthcare Diagnostics Inc, IMC 23-04, IMMULITE® 2000 Thryoglobulin
The purpose of this communication is to inform you of an issue with the product indicated in Table 1 above and provide ...
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GE Medical Systems Information Technologies, Inc., FMI 37206, B125P.B105P.B125M.B105M.B155M Patient Monitor
GE Healthcare is zich ervan bewust dat als bepaalde B1x5P / B1x5M patiëntmonitoren "mmHg" of "kPa" gebruiken als de eenheid voor ...
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GENERI BIOTECH s.r.o, FSCA_UGT1A1_01_2022, gb PHARM UGT1A1
The list of PCR cyclers in the User Manual contains incorrect information about the possibility of using the Rotor-Gene PCR ...
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Ortho Clinical Diagnostics Inc, CL2022-298, ORTHO VISION and VISION Max Analyzers for BioVue
The purpose of this notification is to inform you of a potential for false positive results during a probe replacement process ...