FDA Device Establishments · JSON-LD · Markdown
FEI 3011308139 · 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 · Status: Active
| FEI Number | 3011308139 |
|---|---|
| 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 |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KGZ |
| Regulation § (21 CFR) | 878.4200 |
| Proprietary names | Catheter Accessories |
Source: openFDA. Public-domain (CC0).