FDA Device Establishments · JSON-LD · Markdown
FEI 2125050 · Manufacture Medical Device · Status: Active
| FEI Number | 2125050 |
|---|---|
| Owner / Operator | Coloplast Corp. (#8010144) |
| Address | 1601 W River Rd N, MINNEAPOLIS, MN, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 2 |
| Product codes (top 20) | NEW, GAM |
| Regulation § (21 CFR) | 878.4840, 878.4493 |
| Proprietary names | Digitex Suture Delivery System |
Source: openFDA. Public-domain (CC0).