# Verax Biomedical Incorporated

FEI: 3005935106
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: Verax Biomedical Incorporated (#10023050)

Address: 2200 West Park Drive Suite 300, Westborough, MA, US



## Products

Total registered: 1
Top product codes: MZC
Regulation §: 866.2560

Proprietary names: Platelet PGDprime Test

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223005935106%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3005935106