| Primary Device ID | 30092237622354 |
| NIH Device Record Key | 1626ed6c-1ab1-47d7-8125-7370002c4e37 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ScripHessco |
| Version Model Number | 672-0028-CH |
| Company DUNS | 827221698 |
| Company Name | COMPASS HEALTH BRANDS CORP. |
| 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 | 00092237622353 [Primary] |
| GS1 | 01092237622352 [Unit of Use] |
| GS1 | 30092237622354 [Package] Contains: 00092237622353 Package: Inner Carton [10 Units] In Commercial Distribution |
| GS1 | 80092237622359 [Package] Package: Master Carton [40 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 | 2021-04-08 |
| Device Publish Date | 2021-03-31 |
| 30092237622361 | ScripHessco Standard 2 x 3.5 Foam |
| 30092237622354 | Standard 1.5 x 2.5 Oval Foam |
| 30092237622347 | ScripHessco Basic 2 x 3.5 Cloth |
| 00092237622193 | SCRIPHESSCO STANDARD 2" X 2" FOAM, 4/PK |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() SCRIPHESSCO 86094172 4537584 Live/Registered |
Scrip, Inc. 2013-10-17 |