| Primary Device ID | 00616784704111 |
| NIH Device Record Key | 115a91b9-5d1d-468b-8b6a-4307c67099cd |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | IV Adminstration Set, 10 mL, Non-Toxic |
| Version Model Number | 7041 |
| Company DUNS | 008124539 |
| Company Name | Dynarex Corporation |
| 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 | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| 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 | 00616784704111 [Primary] |
| GS1 | 00616784704135 [Package] Package: Case [50 Units] In Commercial Distribution |
| GS1 | 00616784704142 [Package] Contains: 00616784704135 Package: Shipper [4 Units] In Commercial Distribution |
| FPA | Set, Administration, Intravascular |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 7 |
| Public Version Date | 2025-08-11 |
| Device Publish Date | 2018-01-06 |