• 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 
 8 
 9 
 > 
 
83 records meeting your search criteria returned- Product Code: GAN Product Problem: Detachment Of Device Component Report Date From: 01/1/2007

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
ETHICON INC. MONOCRYL SUTURE 18"(45CM) 4-0 UND 05/15/2018
ETHICON INC. MONOCRYL SUTURE 18"(45CM) 4-0 UND 05/15/2018
ETHICON INC. MONOCRYL SUTURE 27"(70CM) 3-0 UND 05/11/2018
ETHICON INC. MONOCRYL VIO 27IN USP6-0::S/A P-1 PRIME 04/30/2018
ETHICON INC. MONOCRYL SUTURE 18"(45CM) 4-0 UND 04/27/2018
ETHICON INC. MONOCRYL SUTURE 18"(45CM) 4-0 UND 04/27/2018
ETHICON INC. MONOCRYL VIO 27IN USP2-0::S/A SH PLUS VB 04/27/2018
ETHICON INC. MCRYL VIO 36IN 3-0 S/A FS-2 04/25/2018
ETHICON INC. MCRYL VIO 36IN 3-0 S/A FS-2 04/24/2018
ETHICON INC. MONOCRYL ABS SUR SUT SYN 04/23/2018
-
-