FDA Device Establishments · JSON-LD · Markdown
FEI 3014461810 · Export Device to the United States But Perform No Other Operation on Device · Status: Active
| FEI Number | 3014461810 |
|---|---|
| Owner / Operator | BURAK GLOBAL IC VE DIS TIC LTD STI (#10058392) |
| Address | Sahabiye Mh. Ahmet Pasa Cd., Ahmet Pasa Is Merk. No: 16/701, Kocasinan Kayseri, 38015, TR |
| Mandatory US Agent | FDAbasics |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | GCJ |
| Regulation § (21 CFR) | 876.1500 |
| Proprietary names | PREPERITONEAL DISTENTION BALLOON SYSTEM |
Source: openFDA. Public-domain (CC0).