| Primary Device ID | 00811107020972 |
| NIH Device Record Key | 60f88eda-f3e5-4440-a374-0a6d18ab06a5 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Squid Rx |
| Version Model Number | Back |
| Company DUNS | 018238010 |
| Company Name | PORTABLE THERAPEUTIX |
| 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 | true |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| 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 | 00811107020972 [Primary] |
| IME | Pack, Hot Or Cold, Reusable |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-07-31 |
| Device Publish Date | 2023-07-21 |
| 00811107020996 | Squid Rx - Ankle |
| 00811107020989 | Squid Rx - Large Ankle |
| 00811107020972 | Squid Rx - Back |
| 00811107020965 | Squid Rx - Elbow |
| 00811107020958 | Squid Rx - Knee |
| 00811107020941 | Squid Rx - Leg |
| 00811107020927 | Squid Rx - Large Leg |
| 00811107020903 | Squid Rx - Left Shoulder |
| 00811107020897 | Squid Rx - Right Shoulder |
| 00811107020880 | Squid Rx - Large Left Shoulder |
| 00811107020873 | Squid Rx - Large Right Shoulder |
| 00811107020866 | Squid Rx - Wrist |