• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

  • 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 records meeting your search criteria returned- Product Code: MJN Patient Problem: Hemorrhage/Bleeding Report Date From: 01/1/2019
New Searchexport reports to excelExport to Excel | HelpHelp
ManufacturerBrand NameDate Report Received
LEMAITRE VASCULAR, INC. PRUITT F3 CAROTID SHUNT 01/16/2024
LEMAITRE VASCULAR, INC. PRUITT F3 CAROTID SHUNT 01/16/2024
MICRO THERAPEUTICS, INC. DBA EV3 HYPERGLIDE 02/04/2023
LEMAITRE VASCULAR, INC. PRUITT F3 CAROTID SHUNT 01/26/2023
LEMAITRE VASCULAR, INC. PRUITT F3 CAROTID SHUNT 09/02/2022
STRYKER NEUROVASCULAR CORK TRANSFORM SUPER COMPLIANT 4MM X 7MM - US 06/03/2022
RENOVORX, INC. RENOVOCATH 03/29/2022
MICROVENTION, INC. SCEPTER XC 10/12/2021
THE SPECTRANETICS CORPORATION SPECTRANETICS BRIDGE OCCLUDING BALLOON C 07/21/2021
-
-