| Primary Device ID | 06946725525999 |
| NIH Device Record Key | e1b6b361-867c-46ed-a3b3-dbe3f1b872ce |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Datascope |
| Version Model Number | A0405-SP115PV |
| 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 | 06946725525999 [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 |
| 06946725526064 | A0405-SW203PU |
| 06946725526057 | A0405-SP203PU |
| 06946725526040 | A0405-SP203PV |
| 06946725526033 | A0405-SA203PU |
| 06946725526026 | A0405-SA203PV |
| 06946725526019 | A0405-SW115PU |
| 06946725526002 | A0405-SP115PU |
| 06946725525999 | A0405-SP115PV |
| 06946725525982 | A0405-SA115PU |
| 06946725525975 | A0405-SA115PV |