FDA Device Establishments · JSON-LD · Markdown
FEI 3012336447 · Reprocess Single-Use Device · Status: Active
| FEI Number | 3012336447 |
|---|---|
| Owner / Operator | Shurtape Technologies, LLC (#10086854) |
| Address | 621 US HIGHWAY 1 UNIT A, North Brunswick, NJ, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | FMP |
| Regulation § (21 CFR) | 880.6450 |
| Proprietary names | Stryker |
Source: openFDA. Public-domain (CC0).