FDA Device Establishments · JSON-LD · Markdown
FEI 3003587170 · Manufacture Medical Device · Status: Active
| FEI Number | 3003587170 |
|---|---|
| Owner / Operator | NITTO DENKO CORP. (#9048993) |
| Address | 101, SUNADA, SHIMONOME IWADEYAMA, OHSAKI CITY Miyagi, 989-6493, JP |
| Mandatory US Agent | NITTO DENKO Avecia Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | FQM |
| Regulation § (21 CFR) | 880.5075 |
| Proprietary names | Spidertech tape; Spidertech gentle tape |
Source: openFDA. Public-domain (CC0).