10 results
·
19ms
·
Sources: EU EUDAMED, US FDA
TECHNICON H*1 SYSTEM (MPXI)
FDA 510(k)
FDA Class 2
·Hematology
LEONE SPA
FDA UDI
LEONE SPA·08033707031079·WEB 1ST MOL BANDS W/G8325-03 UL 27
NAR
FDA UDI
NORTH AMERICAN RESCUE, LLC·20842209107296·
VSM VITAL SIGNS MONITOR, MODEL 53000 (VSM 300)
FDA 510(k)
FDA Class 2
·Cardiovascular
Cryotop US
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
LIBERTY CYCLER
FDA Adverse Event
Injury
·FRESENIUS MEDICAL CARE·Product code FKX·May 23, 2014
PROSTAR XL SUTURE-MEDIATED CLOSURE
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·November 30, 2012
INTEGRATED APD SET W/CASSETTE3-PRONG
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·October 5, 2010
Pacemaker Kit, part number AMS4281 Pacemaker Kit, part number AMS4281(A Pacemaker Kit, part number AMS4281(C Pacemaker Kit, part number AMS4281(D
FDA Enforcement
Class II
·Terminated·Windstone Medical Packaging, Inc.·March 8, 2017
Percutaneous Entry Kit, part number TVS4022(D Percutaneous Entry Kit , part number TVS4022(E Percutaneous Entry Kit, part number TVS4022(F
FDA Enforcement
Class II
·Terminated·Windstone Medical Packaging, Inc.·March 8, 2017