| Primary Device ID | 50851891007105 |
| NIH Device Record Key | 3eba1395-f28c-4312-bffb-291339f3d521 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Universal Vial Access Device |
| Version Model Number | YM005 |
| Catalog Number | YM005 |
| Company DUNS | 963361170 |
| Company Name | YUKON MEDICAL, LLC |
| 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 | false |
| 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 | 00851891007100 [Primary] |
| GS1 | 50851891007105 [Package] Contains: 00851891007100 Package: CASE [100 Units] In Commercial Distribution |
| LHI | Set, I.V. Fluid Transfer |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2017-06-12 |
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| 10851891007329 - Arisure | 2024-12-05 13mm Arisure Closed Vial Access Device OC |
| 10851891007350 - Arisure | 2024-12-05 20mm Arisure Closed Vial Access Device OC |
| 10885403221644 - SmartSite | 2023-05-18 SmartSite Vented Vial Access Device |
| 50885403228108 - SmartSite | 2023-05-18 SMARTSITE VIALSHIELD 13MM CLOSED VAD |
| 10885403228117 - SmartSite | 2023-05-18 SmartSite VialShield Closed Vial Access Device |
| 50885403228443 - SmartSite | 2023-05-18 SMARTSITE 13MM VENTED VIAL ACCESS DEVICE |
| 50885403228450 - SmartSite | 2023-05-18 SmartSite Vented Vial Access Device |