FDA Device Establishments · JSON-LD · Markdown
FEI 3006116732 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3006116732 |
|---|---|
| Owner / Operator | KBL GmbH (#10030591) |
| Address | Ringstrasse 24-26, Dernbach Rhineland-Palatinate, 56307, DE |
| Mandatory US Agent | Bentley Biomedical Consulting LLC |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | LEJ |
| Regulation § (21 CFR) | 878.4635 |
| Proprietary names | KBL 7000 alpha hybridSun; KBL 8000 alpha hybridSun; KBL 7900 alpha hybridSun; KBL P9S hybridSun; KBL P9 hybridSun; KBL K5 hybridSun; KBL K7S hybridSun; KBL K7 hybridSun; KBL K9S hybridSun |
Source: openFDA. Public-domain (CC0).