# RHENUS SE & CO. KG

FEI: 3014656749
Status: Active
Establishment types: Export Device to the United States But Perform No Other Operation on Device
Owner/operator: Rhenus SE & Co. KG (#10057982)

Address: Rhenus Platz 1, Holzwickede North Rhine-Westphalia, 59439, DE

Mandatory US Agent: Teleflex Inc.

## Products

Total registered: 1
Top product codes: KOD
Regulation §: 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: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223014656749%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3014656749