FDA Device Establishments · JSON-LD · Markdown
FEI 3003772616 · Manufacture Medical Device · Status: Active
| FEI Number | 3003772616 |
|---|---|
| Owner / Operator | Agfa N.V. (#10058267) |
| Address | MAX PLANCK STRASSE 1, PEISSENBERG Bavaria, D82380, DE |
| Mandatory US Agent | Agfa US Corp · shaeann.cavanagh@agfa.com |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | MQB |
| Regulation § (21 CFR) | 892.1680 |
| Proprietary names | CR HD5 FLFS Cassette; CR HD5 General SR Detector; CR HD5 General Detector; CR MD4R FLFS Set; CR MD4R General Set; CR MD4 General Set HR; CR MD4R General SR Set; DX-G; CR HD5 FLFS Detector; NX 3 |
Source: openFDA. Public-domain (CC0).