| Primary Device ID | 00850958007404 |
| NIH Device Record Key | e72cd886-fa11-4c65-8e64-88e60ad27827 |
| Commercial Distribution Discontinuation | 2016-10-10 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Poly Stim II |
| Version Model Number | 203-484 |
| Catalog Number | 350 |
| Company DUNS | 080930531 |
| Company Name | Compass Richmar, LLC |
| 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 | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |