FDA Device Establishments · JSON-LD · Markdown
FEI 3006606901 · Repack or Relabel Medical Device Manufacture Medical Device · Status: Active
| FEI Number | 3006606901 |
|---|---|
| Owner / Operator | Coloplast Corp. (#8010144) |
| Address | COLOPLAST UTCA 2, NYIRBATOR Szabolcs-Szatmar-Bereg, 4300, HU |
| Mandatory US Agent | COLOPLAST CORP. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | FCE, KNT |
| Regulation § (21 CFR) | 876.5210, 876.5980 |
| Proprietary names | Peristeen Plus |
Source: openFDA. Public-domain (CC0).