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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
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126 records meeting your search criteria returned- Product Code: KNH Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009

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ManufacturerBrand NameDate Report Received
Unknown Manufacturer FILSHIE CLIPS 12/10/2018
FEMCARE - NIKOMED LTD FILSHIE CLIP 11/14/2018
FEMACARE - NIKOMED, LTD. FILSHIE CLIPS 10/25/2018
FEMCARE - NIKOMED LTD FILSHIE CLIP 10/23/2018
HOLOGIC, INC. ADIANA PERMANENT CONTRACEPTION SYSTEM 10/09/2018
Unknown Manufacturer TUBAL LIGATION CLIPS 09/25/2018
Unknown Manufacturer TUBAL LIGATION 09/24/2018
Unknown Manufacturer FILSHIE CLIPS 09/21/2018
GYRUS ACMI, INC FBK DUAL INC. W/TROCAR 8/PK 09/13/2018
Unknown Manufacturer FILSHIE CLIPS 08/17/2018
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