# NUCLEIX LTD.

FEI: 3012885391
Status: Active
Establishment types: Repack or Relabel Medical Device; Manufacture Medical Device
Owner/operator: Nucleix Ltd. (#10088381)

Address: 3 Pekeris Street, Rehovot Central, 7670203, IL

Mandatory US Agent: Nucleix Inc.

## Products

Total registered: 1
Top product codes: MMW
Regulation §: 866.6010

Proprietary names: Bladder EpiCheck

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223012885391%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3012885391