FDA Device Establishments · JSON-LD · Markdown
FEI 3013019894 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3013019894 |
|---|---|
| Owner / Operator | REPROLIFE Inc. (#10054077) |
| Address | 2-5-3-9F Shinjuku, Shinjuku-ku Tokyo, 160-0022, JP |
| Mandatory US Agent | Globizz Corp |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | MQK |
| Regulation § (21 CFR) | 884.6160 |
| Proprietary names | Cryotec (4 pieces) (Blue); Cryotec (10 pieces) (White); Cryotec (10 pieces) (Yellow); Cryotec (10 pieces) (Red); Cryotec (4 pieces) (Red); Cryotec (4 pieces) (White); Cryotec (10 pieces) (Blue); Cryotec (10 pieces) (Green); Cryotec (4 pieces) (Yellow); Cryotec (4 pieces) (Green) |
Source: openFDA. Public-domain (CC0).