# OIVI AS

FEI: 3029906968
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Export Device to the United States But Perform No Other Operation on Device; Manufacture Medical Device
Owner/operator: Oivi AS (#10088795)

Address: Gaustadalleen 21, Oslo, 0349, NO

Mandatory US Agent: QA/RA CONSULTING GROUP, INC.

## Products

Total registered: 1
Top product codes: PJZ
Regulation §: 886.1120

Proprietary names: OFC100L, Oivi Fundus Camera

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223029906968%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3029906968