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
 

 
 
 1 
 2 
 3 
 4 
 > 
 
36 records meeting your search criteria returned- Product Code: FCG Product Problem: Material Perforation Report Date From: 01/1/2019

New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
COOK IRELAND LTD ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEED 02/08/2024
COOK IRELAND LTD ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEED 12/19/2023
COOK IRELAND LTD ECHOTIP ULTRA ENDOSCOPIC ULTRASOUND NEED 12/04/2023
AOMORI OLYMPUS CO., LTD. SINGLE USE ASPIRATION NEEDLE NA-U401SX 11/21/2023
COOK IRELAND LTD ECHOTIP PROCORE HIGH DEFINITION ULTRASOU 10/09/2023
AOMORI OLYMPUS CO., LTD. SINGLE USE ASPIRATION NEEDLE 08/30/2023
AOMORI OLYMPUS CO., LTD. SINGLE USE ASPIRATION NEEDLE NA-U401SX 08/24/2023
AOMORI OLYMPUS CO., LTD. SINGLE USE ASPIRATION NEEDLE NA-U401SX 08/21/2023
AOMORI OLYMPUS CO., LTD. SINGLE USE ASPIRATION NEEDLE NA-U401SX 08/01/2023
AOMORI OLYMPUS CO., LTD. SINGLE USE ASPIRATION NEEDLE 07/21/2023
-
-