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Crédits
Devices
Device Recall WellHome Monitor
Modèle / numéro de série
Serial numbers WFD5373, WFD5374, WFD5375, WFD5376, WFD5377, WFD5378, WFD5379,WFD5380, WFD5381, WFD5382, WFD5383, WFD5384, WFD5385, WFD5386, WFD5387, WFD5388, WFD5389, WFD5390, WFD5392, WFD5393, WFD5394,WFD5395, WFD5396, WFD5398, WFD5399, WFD5400, WFD5401, WFD5402, WFD5403, WFD5404, WFD5405, WFD5406, WFD5407, WFD5408, WFD5409,WFD5410, WFD5411, WFD5412, WFD5413, WFD5414, WFD5415, WFD5416, WFD5417, WFD5418, WFD5419, WFD5420, WFD5421, WFD5422, WFD5423,\/VFD5424, VVFD5425, WFD5426, WFD5427, WFD5428, WFD5429, WFD5431, WFD5432, WFD5435, WFD5436, WFD5437, WFD5438, and WFD5439.
Classification du dispositif
Cardiovascular Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Nationwide Distribution -- MA and MD.
Description du dispositif
The Well@Home Monitor by Patient Care technologies || Model 179-2150 || Intended to be used as a clinical tool for remotely monitoring a patient's health status at home or in another healthcare facility on a spot check basis.
Manufacturer
Zoe Medical Incorporated
1 Event
Rappel de Device Recall WellHome Monitor
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Fabricant
Zoe Medical Incorporated
Adresse du fabricant
Zoe Medical Incorporated, 460 Boston St, Topsfield MA 01983-1223
Société-mère du fabricant (2017)
Zoe Medical Incorporated
Source
USFDA
Language
English
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