| Primary Device ID | 00840682146159 | 
| NIH Device Record Key | 19fee96d-2291-46f0-b95a-191c6cd45a12 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Revolution | 
| Version Model Number | Ace | 
| Company DUNS | 654659689 | 
| Company Name | Hangwei GE Medical Systems Co., Ltd. | 
| 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 | true | 
| 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 | true | 
| OTC Over-The-Counter | false | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00840682146159 [Primary] | 
| JAK | System, x-ray, tomography, computed | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2019-11-12 | 
| Device Publish Date | 2019-11-04 | 
| 00840682146180 | Maxima | 
| 00840682146159 | Ace | 
| 00840682146197 | ACT LMB | 
| 00840682137553 | Frontier | 
| 00840682135313 | ACT | 
| 00840682147392 | Revolution Maxima CT designated medical device, WSO make | 
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| 00195278362247 | Revolution Frontier ES for EOL CT Designated medical device | 
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| 00195278943934 | Revolution Vibe - Designated System Medical Device | 
| 00198953049631 | Revolution Maxima CT designated medical device for India, without SGB Tube |