Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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
 

 
 < 
 7 
 8 
 9 
 10 
 11 
 12 
 13 
 14 
 15 
 16 
 > 
 
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
BIOTRONIK SE & CO. KG IFORIA 3 DR-T DF-1 10/16/2018
BIOTRONIK SE & CO. KG IPERIA 7 DR-T DF-1 PROMRI 08/20/2018
BIOTRONIK SE & CO. KG LUMAX 740 DR-T 08/13/2018
SORIN GROUP ITALIA S.R.L. - CRM FACILITY PLATINIUM 08/07/2018
SORIN GROUP ITALIA S.R.L. - CRM FACILITY PARADYM 07/30/2018
BIOTRONIK SE & CO. KG IFORIA 5 DR-T PROMRI DF-1 06/18/2018
SORIN GROUP ITALIA S.R.L. - CRM FACILITY PARADYM 06/13/2018
BIOTRONIK SE & CO. KG LUMAX 500 DR-T 05/15/2018
BIOTRONIK SE & CO. KG IFORIA 3 DR-T DF-1 05/04/2018
SORIN GROUP ITALIA S.R.L - CRM ORCHESTRA PLUS LINK 04/23/2018
-
-