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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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2 records meeting your search criteria returned- Product Code: FHW Product Problem: Improper Flow or Infusion Report Date From: 01/1/2014
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ManufacturerBrand NameDate Report Received
COLOPLAST A/S TITAN SCROTAL ZERO ANG 20CM 12/31/2019
COLOPLAST A/S TITAN TOUCH SCRO ZERO ANG 18CM 12/04/2019
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