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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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138 records meeting your search criteria returned- Product Code: KDI Product Problem: Disconnection Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
BAXTER HEALTHCARE CORPORATION PRISMAFLEX SET 06/08/2020
BAXTER HEALTHCARE CORPORATION PRISMAFLEX HF1000 04/03/2020
BAXTER HEALTHCARE CORPORATION PRISMAFLEX HF1000 03/31/2020
BAXTER HEALTHCARE CORPORATION PRISMAFLEX HF1000 03/23/2020
BAXTER HEALTHCARE CORPORATION PRISMAFLEX HF1400 02/03/2020
BAXTER HEALTHCARE CORPORATION PRISMAFLEX M100 12/23/2019
BAXTER HEALTHCARE CORPORATION PRISMAFLEX M150 12/16/2019
BAXTER HEALTHCARE - MEYZIEU PRISMAFLEX HF1400 12/13/2019
NXSTAGE MEDICAL, INC. NXSTAGE SYSTEM ONE 11/26/2019
BAXTER HEALTHCARE - MEYZIEU NI 09/10/2019
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