FDA Device Establishments · JSON-LD · Markdown
FEI 3016579901 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3016579901 |
|---|---|
| Owner / Operator | Sunphoria Co., Ltd. (#10062637) |
| Address | 12F-1, No.51, Hengyang Rd.,, Zhongzheng Dist.,, Taipei City, 10045, TW |
| Mandatory US Agent | Hikari Dx, Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | ORG |
| Regulation § (21 CFR) | 864.9245 |
| Proprietary names | AHC Platelet Concentrate Separator |
Source: openFDA. Public-domain (CC0).