Establishment registration
NINGBO MPF MANUFACTURING CO.,LTD.
FDA establishment registration 3013180212 · Ningbo Zhejiang, CN
Key facts
| Registration number | 3013180212 |
|---|---|
| Establishment name | NINGBO MPF MANUFACTURING CO.,LTD. |
| Owner/operator | Ningbo MPF Manufacturing Co.,Ltd. |
| Owner/operator number | 10055491 |
| FEI number | 3013180212 |
| Address | KeSi Road, Technology & Science Zone, Ninghai , Zhejiang, China |
| City | Ningbo Zhejiang |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | EXE, FMP, FMQ, FQK, HEF, IKX, ILC, ILE, ILH, ILO, ILT, IME, INP, IOD, IPG, IPT, IQE, IQI, IQK, ISA, ISR, ITQ, ITS, ITW, KIA, KNO, KYS, LYG, MDR, MHW and 4 more |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- None UDI devices (GUDID)
- Current Registration current
- None FDA inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device establishment registrations
Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database