FDA Device Establishments · JSON-LD · Markdown
FEI 3006993432 · Manufacture Medical Device Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active
| FEI Number | 3006993432 |
|---|---|
| Owner / Operator | HL RUBBER INDUSTRIES SDN BHD (#9090472) |
| Address | LOT 10, KAWASAN, PERINDUSTRIAN DIOH, KUALA PILAH Negeri Sembilan, 72000, MY |
| Mandatory US Agent | Elizabeth Deng |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | LYY |
| Regulation § (21 CFR) | 880.6250 |
| Proprietary names | POWDER-FREE LATEX EXAMINATION GLOVES, NON-STERILE; POWDERED LATEX PATIENT EXAMINATION; POWDER-FREE PATIENT EXAMINATION GL; N GLOVE |
Source: openFDA. Public-domain (CC0).