# MEDIPLUS LTD.

FEI: 3011308139
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Develop Specifications But Do Not Manufacture At This Facility; Export Device to the United States But Perform No Other Operation on Device
Owner/operator: MEDIPLUS LTD. (#9041147)

Address: UNIT 7 THE GATEWAY CENTRE, CORONATION RD CRESSEX BUS. PK., HIGH WYCOMBE, BUCKS Buckinghamshire, HP12 3SU, GB

Mandatory US Agent: Promedic, LLC

## Products

Total registered: 1
Top product codes: KGZ
Regulation §: 878.4200

Proprietary names: Catheter Accessories

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223011308139%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3011308139