FDA Device Establishments · JSON-LD · Markdown
FEI 3003282815 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active
| FEI Number | 3003282815 |
|---|---|
| Owner / Operator | MERIDIAN AG (#8030988) |
| Address | BIERIGUTSTRASSE 7, THUN Bern, CH-3608, CH |
| Mandatory US Agent | Regulatory Insight, Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HQF |
| Regulation § (21 CFR) | 886.4390 |
| Proprietary names | MR Q; MR Q Supine; MR Q SLT |
Source: openFDA. Public-domain (CC0).