| Primary Device ID | 00840117310223 |
| NIH Device Record Key | ce07d189-9d3a-4076-87ad-818bd39c54c5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Pulse Oximeter |
| Version Model Number | 36402 |
| Company DUNS | 008124539 |
| Company Name | DYNAREX CORPORATION |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| 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 | false |
| 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 | 00840117310223 [Primary] |
| GS1 | 00840117310230 [Package] Package: Master Case [10 Units] In Commercial Distribution |
| GS1 | 00840117336230 [Package] Contains: 00840117310230 Package: Shipper [1 Units] In Commercial Distribution |
| DQA | Oximeter |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-12-30 |
| Device Publish Date | 2021-12-22 |
| 00616784709031 | 7090 |
| 00616784708935 | 7089 |
| 00616784708836 | 7088 |
| 00840117310223 | Pulse Oximeter, Pediatric |
| 00840117310162 | Pulse Oximeter |