FDA Device Establishments · JSON-LD · Markdown
FEI 3006988008 · Manufacture Medical Device · Status: Active
| FEI Number | 3006988008 |
|---|---|
| Owner / Operator | ALIFAX SRL (#10035224) |
| Address | Via Merano 30, Nimis Udine, 33045, IT |
| Mandatory US Agent | ISOPLAN USA |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | GKB |
| Regulation § (21 CFR) | 864.5800 |
| Proprietary names | SI 305.402-A LATEX CALIBRATORS; SI 305.302-A LATEX CONTROLS (30 TESTS); SI 305.100-A LATEX CONTROLS (6 TESTS); SI 804.100 JO-PLUS; SI 305.400-A LATEX CALIBRATORS; SI 195.210/THL TEST1 2; SI R20-PN ROLLER 20; SI R20-MC ROLLER 20; SI 305.300-A LATEX CONTROLS (30 TESTS); SI 305.102-A LATEX CONTROLS (6 TESTS) |
Source: openFDA. Public-domain (CC0).