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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
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11 records meeting your search criteria returned- Product Code: MZI 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 HUMAN LEUKOCYTE ANTIGEN ANTIBODY TEST 06/11/2021
IMMUCOR GTI DIAGNOSTICS, INC. DONORSCREEN-HLA CLASS I AND CLASS II 07/20/2018
IMMUCOR GTI DIAGNOSTICS, INC. LIFECODES HLA-DRB1 SSO TYPING KIT 06/29/2018
IMMUCOR GTI DIAGNOSTICS, INC. DONOR SCREEN HLA CLASS I AND CLASS II 06/29/2018
IMMUCOR GTI DIAGNOSTICS, INC. DONORSCREEN-HLA CLASS I AND CLASS II 05/24/2018
IMMUCOR GTI DIAGNOSTICS, INC. DONORSCREEN-HLA CLASS I AND CLASS II 05/24/2018
IMMUCOR GTI DIAGNOSTICS, INC. LIFECODES LIFESCREEN DELUXE 11/22/2016
IMMUCOR GTI DIAGNOSTICS, INC. LIFECODES LIFESCREEN DELUXE 11/17/2016
IMMUCOR GTI DIAGNOSTICS, INC. LIFECODES LIFESCREEN DELUXE 11/15/2016
IMMUCOR GTI DIAGNOSTICS, INC. DONORSCREEN-HLA CLASS I AND CLASS II ASS 08/15/2014
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