• 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
 

 
 < 
 1 
 2 
 3 
 4 
 5 
 6 
 7 
 > 
 
64 records meeting your search criteria returned- Product Code: GAW Product Problem: Material Twisted/Bent Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
B. BRAUN SURGICAL, S.A. OPTILENE 3/0 (2) 120CM 2XHR26 CV RCP 03/26/2021
B. BRAUN SURGICAL, S.A. OPTILENE 6/0 (0,7) 75CM 2XDR13B CV2 RCP 03/26/2021
B. BRAUN SURGICAL, S.A. OPTILENE 5/0 (1) 90CM 2XDR13 CV RCP 03/26/2021
B. BRAUN SURGICAL, S.A. OPTILENE 5/0 (1) 90CM 2XDR13 CV2 RCP 03/26/2021
B. BRAUN SURGICAL, S.A. OPTILENE 3/0 (2) 90CM 2XHR26 CV RCP 03/26/2021
B. BRAUN SURGICAL, S.A. OPTILENE 4/0 (1,5) 75CM 2XDR13 CV RCP 12/03/2020
COVIDIEN LP LLC NORTH HAVEN SURGIPRO LL 07/08/2020
B. BRAUN SURGICAL, S.A. OPTILENE 2/0 (3) 75CM HR30 (M) RCP 05/01/2020
B.BRAUN SURGICAL SA OPTILENE 1 (4) 100CM HR40 (M) RCP 03/16/2020
DAVIS & GECK CARIBE LTD SURGIPRO LL 02/10/2020
-
-