| Primary Device ID | 07640142190516 |
| NIH Device Record Key | 25b5e83f-521b-4bff-8a2b-b72a168602a1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | EasyOne FlowTube |
| Version Model Number | 5050-200 |
| Company DUNS | 487451916 |
| Company Name | NDD Medizintechnik AG |
| Device Count | 200 |
| 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 | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07640142190448 [Primary] |
| GS1 | 07640142190455 [Primary] |
| GS1 | 07640142190516 [Unit of Use] |
| BYP | Mouthpiece, Breathing |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-06-30 |
| Device Publish Date | 2023-06-22 |
| 07640142190462 | 5050-500 |
| 07640142190516 | 5050-200 |