FDA Device Establishments · JSON-LD · Markdown
FEI 3020778 · Manufacture Medical Device · Status: Active
| FEI Number | 3020778 |
|---|---|
| Owner / Operator | Procedure Products, Inc. (#3020778) |
| Address | 1801 WEST 4TH PLAIN BLVD., Vancouver, WA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | DRE |
| Regulation § (21 CFR) | 870.1310 |
| Proprietary names | Ultra Modified Seldinger, U-KSDN 19 ga. Special , U-SDN 19 ga. Special; Legths 1.50 to 9 in., Accepts 15 to 38 wires; SDN 18 ga., 19 ga., 21 ga., Special Procedure; Ampllatz, BSDN 18 ga., 19 ga., Modified Potts Cournand, KSDN 18 ga.,; Modified Seldinger Arterial, Chiba, Seldinger without plate, Potts Cournand,; Needles, Single Use Catheterization |
Source: openFDA. Public-domain (CC0).