FDA Device Establishments · JSON-LD · Markdown
FEI 3002806731 · Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3002806731 |
|---|---|
| Owner / Operator | Coloplast Corp. (#8010144) |
| Address | HOLTEDAM 1, HUMLEBAEK Hovedstaden, DK-3050, DK |
| Mandatory US Agent | COLOPLAST CORP. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | EZD |
| Regulation § (21 CFR) | 876.5130 |
| Proprietary names | SpeediCath Compact Male; SpeediCath Compact Male Kit |
Source: openFDA. Public-domain (CC0).