| Primary Device ID | 10199874723973 |
| NIH Device Record Key | 3c78a628-bb3c-45c6-8dd7-ae5361c8c853 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Tournisec |
| Version Model Number | KFG112 |
| Company DUNS | 129718808 |
| Company Name | 62K SOLUTIONS, LLC |
| Device Count | 10 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | false |
| OTC Over-The-Counter | true |
| Phone | 9788917836 |
| customerservice@tournisec.com | |
| Phone | 9788917836 |
| customerservice@tournisec.com | |
| Phone | 9788917836 |
| customerservice@tournisec.com | |
| Phone | 9788917836 |
| customerservice@tournisec.com | |
| Phone | 9788917836 |
| customerservice@tournisec.com |
| Width | 12 Inch |
| Width | 12 Inch |
| Width | 12 Inch |
| Width | 12 Inch |
| Width | 12 Inch |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00199874682402 [Primary] |
| GS1 | 10199874723973 [Unit of Use] |
| ILG | Stocking, Elastic |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-12-23 |
| Device Publish Date | 2025-12-15 |
| 10199874682409 | 10 Pack - Disposable, non-sterile, single use, form fitting, stockinette worn by patient that ac |
| 10199874723973 | 10 Pack - Disposable, non-sterile, single use, form fitting, stockinette worn by patient that ac |