| Primary Device ID | G549SUPREME0 |
| NIH Device Record Key | 34f48b93-2cd1-4786-980c-daebf883dd0f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | EXPRESSION |
| Version Model Number | SUPREME |
| Company DUNS | 119066352 |
| Company Name | Rcs Management Corp |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | MR Unsafe |
| 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 | true |
| Donation Id Number | true |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | G549SUPREME0 [Primary] |
| ILQ | System, Communication, Powered |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-11-29 |
| Device Publish Date | 2024-11-21 |
| G549ULTRA0 | ULTRA |
| G549SUPREME0 | SUPREME |
| G549MINI0 | MINI |
| G549MICRO0 | MICRO |
| G549CLASSIC0 | CLASSIC |