FDA Device Establishments · JSON-LD · Markdown
FEI 3014656749 · Export Device to the United States But Perform No Other Operation on Device · Status: Active
| FEI Number | 3014656749 |
|---|---|
| Owner / Operator | Rhenus SE & Co. KG (#10057982) |
| Address | Rhenus Platz 1, Holzwickede North Rhine-Westphalia, 59439, DE |
| Mandatory US Agent | Teleflex Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KOD |
| Regulation § (21 CFR) | 876.5130 |
| Proprietary names | Rusch all purpose red rubber;; Nelaton-Robinson catheter, cylindrical; Nelaton-Robinson catheter, Tiemann pattern;; Nelaton catheter rubber, cylindrical / Robinson pattern / whistle tip / coaxial / Tiemann pattern;; ERU Catheter PVC Tiemann Pattern; Female catheter;; Rusch all purpose Robinson / Nelation; Rusch Silicone Coated Foley, and pediatric; |
Source: openFDA. Public-domain (CC0).