# VISARIS D.O.O.

FEI: 3012569470
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: Visaris d.o.o. (#10051372)

Address: Batajnicki drum 10. deo 1B, Zemun Beograd, 11080, RS

Mandatory US Agent: Kamm & Associates

## Products

Total registered: 2
Top product codes: KPR, LLZ
Regulation §: 892.1680, 892.2050

Proprietary names: Avanse, LuminX DR Retrofit, Avanse DR, ddRAura DRive Kit

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223012569470%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3012569470