FDA Device Establishments · JSON-LD · Markdown
FEI 3003192903 · Manufacture Medical Device · Status: Active
| FEI Number | 3003192903 |
|---|---|
| Owner / Operator | Hubert De Backer n.v. (#10032923) |
| Address | Laagstraat 59, Temse Oost-Vlaanderen, 9140, BE |
| Mandatory US Agent | P/L Biomedical |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KYX |
| Regulation § (21 CFR) | 880.6430 |
| Proprietary names | T2248; T2188+T2187; T2249; T2044+T2043/A; T2120+T2064/A; T1959; T1630/2B; T1703/1+T2194/1; T2148/1; T1631/1 |
Source: openFDA. Public-domain (CC0).