| Primary Device ID | 07340153710306 |
| NIH Device Record Key | 9e3049f3-ddb6-401d-aceb-0ca8abad1a2a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | GETINGE 6000 |
| Version Model Number | TYPHOON |
| Catalog Number | SP6000AR003 |
| Company DUNS | 354023236 |
| Company Name | Getinge Disinfection AB |
| 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 | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| 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 |