| Primary Device ID | 00616784191614 |
| NIH Device Record Key | 1387b8ed-2f11-4d81-b4c1-9642202a94f0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DynaFit Graduated Compression Anti-Embolism Stocking, Large Thigh |
| Version Model Number | 1916 |
| Company DUNS | 008124539 |
| Company Name | Dynarex Corporation |
| Device Count | 1 |
| 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 | false |
| 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 | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00616784191614 [Primary] |
| GS1 | 00616784191621 [Package] Package: Box [12 Units] In Commercial Distribution |
| GS1 | 00616784191638 [Package] Contains: 00616784191621 Package: Case [5 Units] In Commercial Distribution |
| FQL | Stocking, Medical Support (For General Medical Purposes) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-10-06 |
| Device Publish Date | 2025-09-26 |