| Primary Device ID | 00863520000345 | 
| NIH Device Record Key | 39beb34a-434f-4867-9399-84c07bda2f37 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Synopsys Simpleware ScanIP | 
| Version Model Number | P-2019.09 | 
| Company DUNS | 161499579 | 
| Company Name | SYNOPSYS, INC. | 
| 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 | false | 
| Serial Number | false | 
| Manufacturing Date | false | 
| 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 | 
| Phone | +4401392428750 | 
| simpleware@synopsys.com | |
| Phone | +4401392428750 | 
| simpleware@synopsys.com | |
| Phone | +4401392428750 | 
| simpleware@synopsys.com | |
| Phone | +4401392428750 | 
| simpleware@synopsys.com | |
| Phone | +4401392428750 | 
| simpleware@synopsys.com | |
| Phone | +4401392428750 | 
| simpleware@synopsys.com | |
| Phone | +4401392428750 | 
| simpleware@synopsys.com | |
| Phone | +4401392428750 | 
| simpleware@synopsys.com | |
| Phone | +4401392428750 | 
| simpleware@synopsys.com | |
| Phone | +4401392428750 | 
| simpleware@synopsys.com | |
| Phone | +4401392428750 | 
| simpleware@synopsys.com | |
| Phone | +4401392428750 | 
| simpleware@synopsys.com | |
| Phone | +4401392428750 | 
| simpleware@synopsys.com | |
| Phone | +4401392428750 | 
| simpleware@synopsys.com | |
| Phone | +4401392428750 | 
| simpleware@synopsys.com | |
| Phone | +4401392428750 | 
| simpleware@synopsys.com | |
| Phone | +4401392428750 | 
| simpleware@synopsys.com | |
| Phone | +4401392428750 | 
| simpleware@synopsys.com | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00863520000345 [Primary] | 
| LLZ | System, Image Processing, Radiological | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2019-09-17 | 
| Device Publish Date | 2019-09-09 | 
| 00863520000338 | O-2018.12 | 
| 00863520000345 | P-2019.09 | 
| 00863520000369 | Q-2020.03 | 
| 00863520000352 | Q-2020.06 |