• 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
 

 
 < 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 16 
 17 
 18 
 > 
 
228 records meeting your search criteria returned- Product Code: MRM Product Problem: Failure to Interrogate Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
SORIN GROUP ITALIA S.R.L. - CRM FACILITY PARADYM 11/23/2017
SORIN GROUP ITALIA S.R.L. - CRM FACILITY PLATINIUM 11/10/2017
SORIN GROUP ITALIA S.R.L. - CRM FACILITY PLATINIUM 10/13/2017
SORIN GROUP ITALIA S.R.L. - CRM FACILITY PLATINIUM 09/28/2017
BIOTRONIK SE & CO. KG LUMAX 540 DR-T 09/20/2017
SORIN GROUP ITALIA S.R.L. - CRM FACILITY PLATINIUM 09/12/2017
BIOTRONIK SE & CO. KG LUMAX 540 DR-T 08/18/2017
SORIN GROUP ITALIA S.R.L. - CRM FACILITY PARADYM 08/18/2017
SORIN GROUP ITALIA S.R.L. - CRM FACILITY PLATINIUM 07/20/2017
SORIN GROUP ITALIA S.R.L. - CRM FACILITY ORCHESTRA 06/30/2017
-
-