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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: KDI Patient Problem: Injury Report Date From: 01/1/2018
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ManufacturerBrand NameDate Report Received
BAXTER HEALTHCARE CORPORATION PRISMAFLEX 02/04/2021
BAXTER HEALTHCARE CORPORATION PRISMAFLEX 01/13/2021
GAMBRO AB PRISMAFLEX 03/18/2020
BAXTER HEALTHCARE CORPORATION PRISMAFLEX 11/21/2019
BAXTER HEALTHCARE - HECHINGEN BADEN DIAL REVACLEAR 400 09/25/2019
BAXTER HEALTHCARE - MEYZIEU PRISMAFLEX HF1000 02/07/2019
BAXTER HEALTHCARE - MEYZIEU PRISMAFLEX M100 SET 02/06/2019
BAXTER HEALTHCARE - MEYZIEU PRISMAFLEX M60 SET 02/05/2019
NXSTAGE MEDICAL, INC. NXSTAGE SYSTEM ONE 01/17/2019
BAXTER HEALTHCARE - LUND MONITORS PRISMAFLEX 11/27/2018
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