FDA Device Establishments · JSON-LD · Markdown
FEI 3003502083 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active
| FEI Number | 3003502083 |
|---|---|
| Owner / Operator | KENT ELASTOMER PRODUCTS, INC. (#9044738) |
| Address | 7369 PEABODY-KENT RD., Dundee, OH, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | GBW |
| Regulation § (21 CFR) | 878.4200 |
| Proprietary names | K 600 LATEX TUBING; Penrose Drain Non-Sterile; KEP NON-STERILE; THERMOPLASTIC TUBING; KEP NON STERILE |
Source: openFDA. Public-domain (CC0).