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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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4 records meeting your search criteria returned- Product Code: MMH Patient Problem: No Consequences Or Impact To Patient Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
ONEBLOOD, INC. REGULATED SOFTWARE APPLICATION (RSA) 12/24/2019
IMMUCOR, INC. IMMULINK 07/08/2019
DATA INNOVATIONS LLC INSTRUMENT MANAGER SOFTWARE 04/12/2018
EPIC EPIC CPOE AND MDDS DEVICE 09/12/2017
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