FDA Device Establishments · JSON-LD · Markdown

VISARIS D.O.O.

FEI 3012569470 · Manufacture Medical Device · Status: Active

FEI Number3012569470
Owner / OperatorVisaris d.o.o. (#10051372)
AddressBatajnicki drum 10. deo 1B, Zemun Beograd, 11080, RS
Mandatory US AgentKamm & Associates
Registration expiry2026
Initial importer flagN
Registered products2
Product codes (top 20)KPR, LLZ
Regulation § (21 CFR)892.1680, 892.2050
Proprietary namesAvanse; LuminX DR Retrofit; Avanse DR; ddRAura DRive Kit

External sources

Source: openFDA. Public-domain (CC0).