# FUJIFILM SONOSITE,INC.

FEI: 3002087856
Status: Active
Establishment types: Remanufacture Medical Device; Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: FUJIFILM CORPORATION (#8031568)

Address: 21919 30th Dr SE, BOTHELL, WA, US



## Products

Total registered: 3
Top product codes: ITX, IYN, IYO
Regulation §: 892.1570, 892.1550, 892.1560

Proprietary names: SonoSite Vevo MD Imaging System, Vevo MD Imaging System, FUJIFILM SonoSite Vevo MD Imaging System

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223002087856%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3002087856