FDA Device Establishments · JSON-LD · Markdown
FEI 3038138498 · Export Device to the United States But Perform No Other Operation on Device · Status: Active
| FEI Number | 3038138498 |
|---|---|
| Owner / Operator | Synthon B.V. (#10092950) |
| Address | Microweg 22, Nijmegen Gelderland, 6545, NL |
| Mandatory US Agent | Lachman Consultant Services, Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KZH |
| Regulation § (21 CFR) | 880.6920 |
| Proprietary names | GripMate |
Source: openFDA. Public-domain (CC0).