FDA Device Establishments · JSON-LD · Markdown
FEI 3020163307 · Reprocess Single-Use Device · Status: Active
| FEI Number | 3020163307 |
|---|---|
| Owner / Operator | STRYKER CORP. (#1811755) |
| Address | Ave. Todos los santos No. 10802 Col. Leandro Valle, Tijuana Baja California, C.P. 22643, MX |
| Mandatory US Agent | Stryker |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | NLF, DQA |
| Regulation § (21 CFR) | 870.2700 |
| Proprietary names | Reprocessed RD Set |
Source: openFDA. Public-domain (CC0).