• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

  • Print
  • Share
  • E-mail
-
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
 

 
 
10 records meeting your search criteria returned- Product Code: KDI Patient Problem: Peritonitis Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
BAXTER HEALTHCARE CORPORATION NI 07/12/2022
ERIKA DE REYNOSA, S.A. DE C.V. STAY SAFE MTS SET 12/28/2021
BAXTER HEALTHCARE CORPORATION NI 08/18/2021
NXSTAGE MEDICAL, INC. NXSTAGE SYSTEM ONE 07/01/2021
ERIKA DE REYNOSA, S.A. DE C.V. UNKNOWN- FMC PRODUCT 06/25/2021
BAXTER HEALTHCARE CORPORATION NI 08/28/2020
ERIKA DE REYNOSA, S.A. DE C.V. STAY SAFE/LUER LOCK CATHETER EXT. 18 IN. 01/30/2020
BAXTER HEALTHCARE CORPORATION NI 12/30/2019
ERIKA DE REYNOSA, S.A. DE C.V. STAY SAFE/LUER LOCK CATHETER EXT. 12 IN. 10/14/2019
ERIKA DE REYNOSA, S.A. DE C.V. STAY SAFE/LUER LOCK CATHETER EXT. 18 IN. 04/09/2019
-
-