FDA Device Establishments · JSON-LD · Markdown
FEI 3007134520 · Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3007134520 |
|---|---|
| Owner / Operator | Teleflex (#9062981) |
| Address | IDA BUSINESS AND TECHNOLOGY PARK, DUBLIN ROAD, ATHLONE Westmeath, --, IE |
| Mandatory US Agent | Teleflex, Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | GBM, KOD |
| Regulation § (21 CFR) | 876.5130 |
| Proprietary names | Rusch Flocath Hydrophilic Intermittent Catheter, Rusch MMG Hydrophilic Intermittent Catheter |
Source: openFDA. Public-domain (CC0).