FDA Device Establishments · JSON-LD · Markdown
FEI 3000266850 · Manufacture Medical Device · Status: Active
| FEI Number | 3000266850 |
|---|---|
| Owner / Operator | Petermann GmbH (#10023922) |
| Address | WAldweg 3, Dombuehl Bavaria, 91601, DE |
| Mandatory US Agent | Arjo, Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | IKX |
| Regulation § (21 CFR) | 890.5050 |
| Proprietary names | ArjoHuntleigh Maxionce |
Source: openFDA. Public-domain (CC0).