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

MAUDE - Manufacturer and User Facility Device Experience

  • 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
 

 
 
 1 
 2 
 > 
 
20 records meeting your search criteria returned- Product Code: NRY Product Problem: Mechanical Problem Report Date From: 01/1/2009
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
RAPID MEDICAL LTD. TIGERTRIEVER 05/02/2023
RAPID MADICAL LTD. TIGERTRIEVER 05/01/2023
PENUMBRA, INC. PENUMBRA SYSTEM 3D REVASCULARIZATION DEV 06/06/2019
PENUMBRA, INC. PENUMBRA SYSTEM ASPIRATION PUMP MAX 110 05/08/2019
PENUMBRA, INC. PENUMBRA SYSTEM ASPIRATION PUMP MAX 220 02/15/2019
PENUMBRA, INC. PENUMBRA SYSTEM ASPIRATION PUMP MAX 110 02/08/2019
PENUMBRA, INC. PENUMBRA SYSTEM ASPIRATION PUMP MAX 110 12/18/2018
PENUMBRA, INC. PENUMBRA SYSTEM 5MAX ACE 68 REPERFUSION 10/11/2018
PENUMBRA, INC. PENUMBRA SYSTEM 3MAX REPERFUSION CATHETE 09/28/2018
PENUMBRA, INC. PENUMBRA SYSTEM ACE 68 REPERFUSION CATHE 09/25/2018
-
-