FDA Device Establishments · JSON-LD · Markdown
FEI 3015007456 · Export Device to the United States But Perform No Other Operation on Device Manufacture Medical Device · Status: Active
| FEI Number | 3015007456 |
|---|---|
| Owner / Operator | Shenzhen IMDK Medical Technology Co., Ltd. (#10058601) |
| Address | 904,9F,Guangming Tianan Cloud Park Building,255 Zhenmei Road,Zhenmei Community,Xinhu Street,, Guangming District,518107,Shenzhen,PEOPLE'S REPUBLIC OF CHINA., SHENZHEN Guangdong, 518106, CN |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | DQA |
| Regulation § (21 CFR) | 870.2700 |
| Proprietary names | Pulse Oximeter ;Model:PO-A2AO, PO-A2AT, PO-A3AO, PO-H1AO, PO-B1AO, PO-C5AO, PO-C5AT, PO-C6AO, PO-C6AT |
Source: openFDA. Public-domain (CC0).