FDA Device Establishments · JSON-LD · Markdown
FEI 3001082453 · Manufacture Medical Device · Status: Active
| FEI Number | 3001082453 |
|---|---|
| Owner / Operator | SWEDEN & MARTINA S.p.A. (#10046682) |
| Address | Via Veneto, 10, Due Carrare Padova, 35020, IT |
| Mandatory US Agent | THEMA CORP |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KCT |
| Regulation § (21 CFR) | 880.6850 |
| Proprietary names | SURGICAL KIT; REMOVAL SCREW KIT; KIT D.B.E. SYSTEM; SURGICAL KIT ECHOPLAN PRO; GLOBAL BONE EXPANDER KIT; MOUNTER TRAY ORGANIZER; PREMIUM SUPPLEMENTARY INSTR.; SURGICAL KIT "ONEBOX"; PROSTHETIC ACCESSORIES KIT; OUTLINK2 SUPPLEMENTARY INSTR. |
Source: openFDA. Public-domain (CC0).