| Primary Device ID | 00762860125018 |
| NIH Device Record Key | a9ac9e55-29a1-4508-81f5-99c911311479 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | RespiConnect* Adapter |
| Version Model Number | 112501 |
| Catalog Number | 11250194040 |
| Company DUNS | 203298203 |
| Company Name | Trudell Medical International |
| 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 | 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 | 00762860125018 [Primary] |
| GS1 | 10762860125015 [Package] Package: [40 Units] In Commercial Distribution |
| GS1 | 62860112501020 [Previous] |
| CAF | Nebulizer (Direct Patient Interface) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-02-27 |
| Device Publish Date | 2020-02-19 |
| 62860112501020 | RespiConnect* Adapter |
| 00762860125018 | RespiConnect* Adapter |