| Primary Device ID | 06946725525876 |
| NIH Device Record Key | 3bb900d8-8f71-4f24-b686-8f78b9bd79e7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CSI |
| Version Model Number | A0309-SA202PV |
| Company DUNS | 529691989 |
| Company Name | APK Technology Co.,Ltd. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | true |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06946725525876 [Primary] |
| DQA | Oximeter |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2018-04-10 |
| 06946725525913 | A0309-SW202PU |
| 06946725525906 | A0309-SP202PU |
| 06946725525890 | A0309-SP202PV |
| 06946725525883 | A0309-SA202PU |
| 06946725525876 | A0309-SA202PV |
| 06946725525869 | A0309-SW111PU |
| 06946725525852 | A0309-SP111PU |
| 06946725525845 | A0309-SP111PV |
| 06946725525838 | A0309-SA111PU |
| 06946725525821 | A0309-SA111PV |
| 06946725525814 | A0309-SW102PU |
| 06946725525807 | A0309-SP102PU |
| 06946725525791 | A0309-SP102PV |
| 06946725525784 | A0309-SA102PU |
| 06946725525777 | A0309-SA102PV |