Canadian data is current through March 2018. All of the data comes from Health Canada, except for the categories Manufacturer Parent Company and Product Classification.
The Parent Company and the Product Classification were added by ICIJ.
The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of recall data from the U.S. and Canada.
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St-segments in a 12-lead ecg may become distorted and the st-value may be inaccurate when an affected monitor automatically activates ecg filtering in the event that a "ecg check cable" or "ecg noisy elec xx" inop condition is triggered and displayed.
Model Catalog: M3001A (Lot serial: >100 numbers contact mfg.); Model Catalog: M8102A (Lot serial: >100 numbers contact mfg.); Model Catalog: M8105A (Lot serial: >100 numbers contact mfg.); Model Catalog: M3002A (Lot serial: >100 numbers contact mfg.)
제품 설명
INTELLIVUE PATIENT MONITOR SYSTEM - MULTI MEASUREMENT SERVER;INTELLIVUE MP2 PATIENT MONITOR - MAIN UNIT;INTELLIVUE MP5 PATIENT MONITOR SYSTEM - MAIN UNIT;INTELLIVUE X2 MULTI-MEASUREMENT MODULE - MAIN UNIT