# NEUROLIEF Ltd.

FEI: 3015088397
Status: Active
Establishment types: Export Device to the United States But Perform No Other Operation on Device; Manufacture Medical Device; Complaint File Establishment per 21 CFR 820.198
Owner/operator: Neurolief (#10081665)

Address: 12 Giborei Israel, Netanya Central, 4250412, IL

Mandatory US Agent: Neurolief Inc.

## Products

Total registered: 1
Top product codes: PCC
Regulation §: 882.5891

Proprietary names: Relivion

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223015088397%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3015088397
