FDA Device Establishments · JSON-LD · Markdown

FUJIFILM SONOSITE,INC.

FEI 3002087856 · Remanufacture Medical Device Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active

FEI Number3002087856
Owner / OperatorFUJIFILM CORPORATION (#8031568)
Address21919 30th Dr SE, BOTHELL, WA, US
Registration expiry2026
Initial importer flagN
Registered products3
Product codes (top 20)ITX, IYN, IYO
Regulation § (21 CFR)892.1570, 892.1550, 892.1560
Proprietary namesSonoSite Vevo MD Imaging System; Vevo MD Imaging System; FUJIFILM SonoSite Vevo MD Imaging System

External sources

Source: openFDA. Public-domain (CC0).