FDA Device Establishments · JSON-LD · Markdown
FEI 3000130829 · Manufacture Medical Device Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3000130829 |
|---|---|
| Owner / Operator | Analog Devices (#10089993) |
| Address | One Analog Way, Wilmington, MA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 7 |
| Product codes (top 20) | DSB, MWI, DQD, FLL, DPS, BZQ, DXH |
| Regulation § (21 CFR) | 870.2770, 870.2300, 870.1875, 880.2910, 870.2340, 868.2375, 870.2920 |
| Proprietary names | Sensinel CPM System; Sensinel Intelligent Algorithm; Sensinel CPM Base Station; Sensinel CPM Mobile Application; Sensinel CPM Web Application; Sensinel CPM Wearable; Sensinel CPM Adhesives |
Source: openFDA. Public-domain (CC0).