FDA Device Establishments · JSON-LD · Markdown
FEI 3009608177 · Manufacture Medical Device · Status: Active
| FEI Number | 3009608177 |
|---|---|
| Owner / Operator | Rmedica co., Ltd (#10040716) |
| Address | 2-Dong 709-Ho (Gasan-Dong, IT Castle), 98, Gasan digital 2-ro, Geumcheon-Gu Seoul, 08506, KR |
| Mandatory US Agent | Provision Consulting Group, Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | ORG |
| Regulation § (21 CFR) | 864.9245 |
| Proprietary names | Platelet and Plasma Separator for Bone Graft Handling, GC Dr.PRP; Platelet and Plasma Separator for Bone Graft Handling, Dr.PRP-I; Platelet and Plasma Separator for Bone Graft Handling, Dr.PRP |
Source: openFDA. Public-domain (CC0).