Ventripoint Diagnostics L T D

FDA Filings

This page includes the latest FDA filings for Ventripoint Diagnostics L T D. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

CANADATSX VENTURE EXCHANGEVPTDUNS 243131807
FDA Registration(s)
Registration Number3007194257
FEI Number3007194257
NameVENTRIPOINT DIAGNOSTICS LTD.
Owner & OperatorVentripoint Diagnostics Ltd.
Contact Address2 Sheppard Ave East. Suite 605
Toronto CA-ON Ontario M2N 5Y7 CA
Official Correspondent
  • Alvira Macanovic
  • 1-416-8484156-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address2 Sheppard Avenue East Suite 605
Toronto Ontario, M2N 5Y7 CA
Establishment Type
  • Manufacture Medical Device
  • Complaint File Establishment per 21 CFR 820.198



FDA Filings

Device
Company
DeviceDate
VENTRIPOINT DIAGNOSTICS LTD.
Ventripoint Medical System Plus (Vms+) 3.02020-01-09
VENTRIPOINT DIAGNOSTICS LTD.
Ventripoint Medical System Plus (Vms+) 3.02020-01-09
VENTRIPOINT DIAGNOSTICS LTD.
Ventripoint Medical System Plus (Vms+) 3.02020-01-09
VENTRIPOINT DIAGNOSTICS LTD.
Ventripoint Medical System Plus (Vms+) 3.02020-01-09
Ventripoint Diagnostics, Ltd.
Ventripoint Medical System Plus (VMS+) 3.02019-10-16
VentriPoint Diagnostics Ltd
Ventripoint Medical System Plus (VMS+) 2018-12-10
VENTRIPOINT DIAGNOSTICS LTD.
Ventripoint Medical System Plus (VMS+)2018-06-08
Ventripoint Diagnostics, Ltd.
Ventripoint Medical System Plus (VMS+)2018-05-14
VENTRIPOINT DIAGNOSTICS LTD.
VentriPoint Medical System2014-04-18

Related Finance Registrations

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.