FDA Device Establishments · JSON-LD · Markdown
FEI 3012649202 · Export Device to the United States But Perform No Other Operation on Device · Status: Active
| FEI Number | 3012649202 |
|---|---|
| Owner / Operator | Coloplast Corp. (#8010144) |
| Address | 2 Rue Jacqueline Auriol, Le Plessis-Pate Essonne, 91220, FR |
| Mandatory US Agent | COLOPLAST CORP |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | FED |
| Regulation § (21 CFR) | 876.1500 |
| Proprietary names | ReTrace Ureteral Access Sheath |
Source: openFDA. Public-domain (CC0).