| Primary Device ID | 00860009591530 |
| NIH Device Record Key | 7fad6814-0c3b-4ee7-8648-7b5692a21717 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Lung Diffusion Mixtures |
| Version Model Number | 1 |
| Company DUNS | 005436332 |
| Company Name | Ilmo Products Company |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | false |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00860009591530 [Primary] |
| BXK | Gas, Calibration (Specified Concentration) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-12-06 |
| Device Publish Date | 2022-11-28 |
| 00860009591509 - Aerobic Mixtures | 2022-12-06 GAS, CALIBRATION (SPECIFIED CONCENTRATION) - Aerobic Mixtures |
| 00860009591516 - Anaerobic Mixtures | 2022-12-06 GAS, CALIBRATION (SPECIFIED CONCENTRATION) - Anaerobic Mixtures |
| 00860009591523 - Clinical Blood Gas Mixtures | 2022-12-06 GAS, CALIBRATION (SPECIFIED CONCENTRATION) - Clinical Blood Gas Mixtures |
| 00860009591530 - Lung Diffusion Mixtures | 2022-12-06GAS, CALIBRATION (SPECIFIED CONCENTRATION) - Lung Diffusion Mixtures |
| 00860009591530 - Lung Diffusion Mixtures | 2022-12-06 GAS, CALIBRATION (SPECIFIED CONCENTRATION) - Lung Diffusion Mixtures |