FDA Device Establishments · JSON-LD · Markdown
FEI 3010898856 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3010898856 |
|---|---|
| Owner / Operator | G21 s.r.l. (#10051231) |
| Address | Via S. Pertini, 8, San Possidonio Modena, 41039, IT |
| Mandatory US Agent | Regulatory/Quality Management Information Source, Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HTC |
| Regulation § (21 CFR) | 878.4800 |
| Proprietary names | CeMend Cemet Mold Pilers |
Source: openFDA. Public-domain (CC0).