FDA Device Establishments · JSON-LD · Markdown
FEI 3017618900 · Develop Specifications But Do Not Manufacture At This Facility Export Device to the United States But Perform No Other Operation on Device Foreign Private Label Distributor Manufacture Medical Device for Another Party (Contract Manufacturer) Repack or Relabel Medical Device Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3017618900 |
|---|---|
| Owner / Operator | Huizhou Gold Rose Technology Co.,Ltd (#10078391) |
| Address | LEFT 2ND FLOOR, NO.3 LEJIN NORTH ROAD, NO.24 DISTRICT, ZHONGKAI DEVELOPMENT ZONE, huizhou Guangdong, 516000, CN |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KMY |
| Regulation § (21 CFR) | 872.5525 |
Source: openFDA. Public-domain (CC0).