Without the benefit of examination and testing, coloplast is precluded from commenting on the condition of the device or the cause of the occurrence.Should additional facts prompt us to alter or supplement any information of conclusions contained in the original mdr or in any prior supplemental reports, a follow-up report will be submitted.
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According to the available information, medwatch 5071730 - patient experienced urge incontinence, sexual pain and right leg pain, bad low detrusor capacity, constipation, irritable bowel.
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