FDA Device Establishments · JSON-LD · Markdown
FEI 3016927399 · Manufacture Medical Device Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active
| FEI Number | 3016927399 |
|---|---|
| Owner / Operator | REPROLIFE Inc. (#10073837) |
| Address | 26-1 Hara, Numazu Shizuoka, 410-0312, JP |
| Mandatory US Agent | Globizz Corporation |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | PUD |
| Regulation § (21 CFR) | 884.6160 |
| Proprietary names | Vitri Plate-10 Plates; Warm Plate-10 Plates |
Source: openFDA. Public-domain (CC0).