FDA Device Establishments · JSON-LD · Markdown
FEI 3007075140 · Manufacture Medical Device Export Device to the United States But Perform No Other Operation on Device · Status: Active
| FEI Number | 3007075140 |
|---|---|
| Owner / Operator | YELATMA INSTRUMENT-MAKING ENTERPRISE (#10026579) |
| Address | 25 Yanina Street, Yelatma, Ryazan Ryazanskaya Oblast', 391351, RU |
| Mandatory US Agent | Almagia International |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HCC |
| Regulation § (21 CFR) | 882.5050 |
| Proprietary names | ALMAG 02 Biofeedback Device; ALMAG 01 Biofeedback Device; POLYMAG Biofeedback Device; ALMAG PLUS Biofeedback Device; ALMAG 03 (DIAMAG) Biofeedback Device; ALMAG ACTIVE Biofeedback Device |
Source: openFDA. Public-domain (CC0).