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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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10 records meeting your search criteria returned- Product Code: NQM Patient Problem: No Known Impact Or Consequence To Patient Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
QIAGEN SCIENCES, LLC AMNISURE ROM TEST 02/24/2020
QIAGEN SCIENCES, LLC AMNISURE ROM TEST 02/24/2020
QIAGEN SCIENCES, LLC AMNISURE ROM TEST 02/19/2020
QIAGEN SCIENCES, LLC AMNISURE ROM TEST 02/19/2020
QIAGEN SCIENCES, LLC AMNISURE ROM TEST 02/19/2020
QIAGEN SCIENCES, LLC AMNISURE ROM TEST 04/29/2019
CLINICAL INNOVATIONS EUROPE, LTD. ROM PLUS COMPLETE KIT 10/01/2018
QIAGEN SCIENCES, LLC AMNISURE ROM TEST 05/14/2018
QIAGEN SCIENCES, LLC AMNISURE ROM TEST 03/16/2018
QIAGEN GMBH AMNISURE ROM 02/16/2018
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