FDA Device Establishments · JSON-LD · Markdown
FEI 3040096051 · Manufacture Medical Device · Status: Active
| FEI Number | 3040096051 |
|---|---|
| Owner / Operator | M.I.Tech Co., Ltd. (#10030918) |
| Address | 17-3 Palbok 1-Gil, Deokjin District, Jeonju Jeonbuk, 54883, KR |
| Mandatory US Agent | LK Consulting Group USA, Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | MQR |
| Regulation § (21 CFR) | 878.3610 |
| Proprietary names | HANAROSTENT LowAX Colon/Rectum(NNN); HANAROSTENT LowAx Duodenum/Pylorus(NNN) |
Source: openFDA. Public-domain (CC0).