| Primary Device ID | 80092237900938 |
| NIH Device Record Key | d6a116ba-d8a7-4de0-9dd7-4a3f4ab0a4e4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | UltraStick - HJ & Associates PL |
| Version Model Number | 203-819 |
| Company DUNS | 080930531 |
| Company Name | Compass Richmar, LLC |
| Device Count | 4 |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00092237900932 [Primary] |
| GS1 | 01092237900931 [Unit of Use] |
| GS1 | 30092237900933 [Package] Contains: 00092237900932 Package: Inner Carton [10 Units] In Commercial Distribution |
| GS1 | 80092237900938 [Package] Contains: 30092237900933 Package: Master Carton [30 Units] In Commercial Distribution |
| GXY | Electrode, Cutaneous |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-02-18 |
| Device Publish Date | 2019-01-18 |
| 80092237900952 | 3" Round Cloth |
| 80092237900945 | 2"x 3.5" Cloth |
| 80092237900938 | 3" Round Foam |
| 80092237900921 | 2"x 3.5" Foam |
| 80092237900907 | 2"x 2" Foam |
| 80092237900891 | 2" Round Cloth |
| 80092237900884 | 2" Round Foam |