FDA Device Establishments · JSON-LD · Markdown
FEI 3010760953 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device for Another Party (Contract Manufacturer) Repack or Relabel Medical Device Manufacture Medical Device · Status: Active
| FEI Number | 3010760953 |
|---|---|
| Owner / Operator | Nenesupply Co., Ltd. (#10046640) |
| Address | 2F, No 9, Ln 235, Baoqiao Rd., Xindian District, New Taipei City, 23148, TW |
| Mandatory US Agent | Nenesupply LLC |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | OHH |
| Regulation § (21 CFR) | 884.5160 |
| Proprietary names | Nenesupply Valve + Membrane; Nenesupply Breastpump Kit - Breastshield+Valve+Membrane+Tubing+Bottle; Nenesupply Tubing; Nenesupply Backflow Protector; Nenesupply Valve |
Source: openFDA. Public-domain (CC0).