| Primary Device ID | 00857926006001 |
| NIH Device Record Key | 3cde5750-cf8f-48ab-84a3-6caec4564e2a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | R4 ACERT |
| Version Model Number | 4.20.300 |
| Company DUNS | 787515550 |
| Company Name | HYLAND SOFTWARE, 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 | true |
| 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 | false |
| OTC Over-The-Counter | false |