FDA Device Establishments · JSON-LD · Markdown
FEI 3003191258 · Export Device to the United States But Perform No Other Operation on Device · Status: Active
| FEI Number | 3003191258 |
|---|---|
| Owner / Operator | ASIA-MED GMBH (#9043114) |
| Address | Kirchplatz 1, Pullach i.I. Bavaria, 82049, DE |
| Mandatory US Agent | REGULATORY INSIGHT, INC. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | MQX |
| Regulation § (21 CFR) | 880.5580 |
| Proprietary names | TeWa acupuncture needles; TeWa PJ-Type; TeWa DPB-Type; TeWa 10KB-Type; TeWa CJ-Type Safe-T Sleeve; TeWa JJ-Type; TeWa ID-Type; TeWa CJ-Type; TeWa PB-Type; TeWa 5CB-Type |
Source: openFDA. Public-domain (CC0).