# VENTRIPOINT DIAGNOSTICS LTD.

FEI: 3007194257
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: Ventripoint Diagnostics Ltd. (#10046630)

Address: 18 Hook Avenue, Unit 101, Toronto Ontario, M6P1T4, CA

Mandatory US Agent: PAXMED INTERNATIONAL, LLC

## Products

Total registered: 2
Top product codes: LLZ, QIH
Regulation §: 892.2050

Proprietary names: Ventripoint Medical System Plus (VMS+) 4

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223007194257%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3007194257