# Murata Vios, Inc.

FEI: 3015328411
Status: Active
Establishment types: Remanufacture Medical Device; Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device; Repack or Relabel Medical Device
Owner/operator: Murata Vios, Inc. (#10059850)

Address: 700 Commerce Drive, Suite 190, Woodbury, MN, US



## Products

Total registered: 4
Top product codes: DRT, DRG, DPZ, DQA
Regulation §: 870.2300, 870.2910, 870.2710, 870.2700

Proprietary names: Vios Monitoring System™ Model 2050

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223015328411%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3015328411