| Primary Device ID | 80092237900440 |
| NIH Device Record Key | 57999274-0dc6-4b53-a88c-8112adffc2f0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Medical Science Private Label |
| Version Model Number | 203-493 |
| 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 | 00092237900444 [Primary] |
| GS1 | 01092237900443 [Unit of Use] |
| GS1 | 30092237900445 [Package] Contains: 00092237900444 Package: Inner Carton [10 Units] In Commercial Distribution |
| GS1 | 80092237900440 [Package] Contains: 30092237900445 Package: Master Carton [50 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 | 2019-02-07 |
| Device Publish Date | 2019-01-07 |
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| 10853904006060 - BodyMed Iontophoresis Electrode Kit | 2023-09-25 |
| 10853904006077 - BodyMed Iontophoresis Electrode Kit | 2023-09-25 |
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| 10853904006398 - GelShot | 2022-06-10 GelShot-/Adaptor-Chattanooga Intelect Legend 5 cm, Case of 10 |
| 10850689007312 - STICK-E-PADS | 2021-02-19 1.5"x 3.5" Cloth, Case of 10 |
| 10850689007329 - STICK-E-PADS | 2021-02-19 1.5"x 3.5" Foam, Case of 10 |