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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
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8 records meeting your search criteria returned- Product Code: PNZ Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
ENTELLUS MEDICAL, INC. AUDION 6X20MM 12/02/2022
ACCLARENT, INC. ACCLARENT AERA EUSTACHIAN TUBE BALLOON D 10/03/2022
ACCLARENT, INC. UNKNOWN BALLOON CATHETER 1ST GEN 09/14/2020
ENTELLUS MEDICAL, INC. XPRESS ULTRA ENT DILATION SYSTEM 03/11/2020
ACCLARENT, INC. ACCLARENT AERA EUSTACHIAN TUBE BALLOON D 04/15/2019
ENTELLUS MEDICAL, INC. XPRESS ULTRA ENT DILATION SYSTEM 09/06/2018
ENTELLUS MEDICAL XPRESS LOPROFILE ENT DILATION SYSTEM 04/12/2018
ENTELLUS MEDICAL XPRESS LOPROFILE ENT DILATION SYSTEM 07/24/2017
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