FDA Device Establishments · JSON-LD · Markdown

BIOVIEW LTD.

FEI 3003909093 · Manufacture Medical Device · Status: Active

FEI Number3003909093
Owner / OperatorBIOVIEW LTD. (#9054795)
Address3 PAKRIS STREET, REHOVOT Central, 76702, IL
Mandatory US AgentBIOVIEW USA INC.
Registration expiry2026
Initial importer flagN
Registered products2
Product codes (top 20)NTH, JOY
Regulation § (21 CFR)866.4700, 864.5260
Proprietary namesSolo-Touch Review workstation; SIMP – (“Slide Interface Messaging Protocol”); Solo™ Review workstation; SoloWeb analysis configuration; Allegro Plus; Accord Plus; Encore; Duet-3

External sources

Source: openFDA. Public-domain (CC0).