| Primary Device ID | 00840117342866 |
| NIH Device Record Key | f2050d32-a224-472c-afba-f8c9cd7e1914 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Durma+ Transparent Wound Drape, 12" x 12" |
| Version Model Number | 3129 |
| 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 | 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00840117342842 [Package] Contains: 00840117342859 Package: Case [20 Units] In Commercial Distribution |
| GS1 | 00840117342859 [Package] Package: Box [5 Units] In Commercial Distribution |
| GS1 | 00840117342866 [Primary] |
| KMK | Device, Intravascular Catheter Securement |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-06-11 |
| Device Publish Date | 2025-06-03 |
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| 00616784704111 - IV Adminstration Set, 10 mL, Non-Toxic | 2025-08-11 Sterile-EO |
| 00616784704210 - IV Administration Sets, 10 mL, Non-Toxic | 2025-08-11 Sterile-EO |
| 00616784704418 - IV Administration Set, 20 mL, Non-Toxic | 2025-08-11 Sterile-EO |