| Primary Device ID | 50885403232679 |
| NIH Device Record Key | 1be9bb62-c4fe-4d9a-94bc-3c12e2fd38e1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | None |
| Version Model Number | MV0613 |
| Catalog Number | MV0613 |
| 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 |
| Lumen/Inner Diameter | 13 Millimeter |
| Lumen/Inner Diameter | 13 Millimeter |
| Lumen/Inner Diameter | 13 Millimeter |
| Lumen/Inner Diameter | 13 Millimeter |
| Lumen/Inner Diameter | 13 Millimeter |
| Lumen/Inner Diameter | 13 Millimeter |
| Lumen/Inner Diameter | 13 Millimeter |
| Lumen/Inner Diameter | 13 Millimeter |
| Lumen/Inner Diameter | 13 Millimeter |
| Lumen/Inner Diameter | 13 Millimeter |
| Lumen/Inner Diameter | 13 Millimeter |
| Lumen/Inner Diameter | 13 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10885403232671 [Primary] |
| GS1 | 50885403232679 [Package] Contains: 10885403232671 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 | 3 |
| Public Version Date | 2023-05-18 |
| Device Publish Date | 2017-07-07 |
| 50885403232679 | MALE LUER 13MM VIAL ACCESS DEVICE |
| 50885403232662 | MALE LUER 20MM VIAL ACCESS DEVICE |
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