FDA Device Establishments · JSON-LD · Markdown
FEI 3000191104 · Manufacture Medical Device · Status: Active
| FEI Number | 3000191104 |
|---|---|
| Owner / Operator | OWEN MUMFORD, LTD. (#8021764) |
| Address | BROOK HILL, WOODSTOCK, OXFORDSHIRE, 0X20ITU, GB |
| Mandatory US Agent | OWEN MUMFORD USA, INC |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KZH |
| Regulation § (21 CFR) | 880.6920 |
| Proprietary names | AUTOJECT 2 (NON-FIXED NEEDLE); Betaject Lite; Extavia Auto-Injector II |
Source: openFDA. Public-domain (CC0).