| Primary Device ID | 50851891007037 |
| NIH Device Record Key | 951977ce-206d-4819-b79e-672afa209f6d |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | YM035 |
| Catalog Number | YM035 |
| 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 |
| Phone | 919-595-8250 |
| Quality@YukonMedical.com | |
| Phone | 919-595-8250 |
| Quality@YukonMedical.com | |
| Phone | 919-595-8250 |
| Quality@YukonMedical.com | |
| Phone | 919-595-8250 |
| Quality@YukonMedical.com | |
| Phone | 919-595-8250 |
| Quality@YukonMedical.com | |
| Phone | 919-595-8250 |
| Quality@YukonMedical.com | |
| Phone | 919-595-8250 |
| Quality@YukonMedical.com | |
| Phone | 919-595-8250 |
| Quality@YukonMedical.com | |
| Phone | 919-595-8250 |
| Quality@YukonMedical.com | |
| Phone | 919-595-8250 |
| Quality@YukonMedical.com | |
| Phone | 919-595-8250 |
| Quality@YukonMedical.com | |
| Phone | 919-595-8250 |
| Quality@YukonMedical.com | |
| Phone | 919-595-8250 |
| Quality@YukonMedical.com | |
| Phone | 919-595-8250 |
| Quality@YukonMedical.com | |
| Phone | 919-595-8250 |
| Quality@YukonMedical.com | |
| Phone | 919-595-8250 |
| Quality@YukonMedical.com | |
| Phone | 919-595-8250 |
| Quality@YukonMedical.com | |
| Phone | 919-595-8250 |
| Quality@YukonMedical.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00851891007032 [Primary] |
| GS1 | 50851891007037 [Package] Contains: 00851891007032 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 | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-11-22 |
| Device Publish Date | 2018-10-22 |
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| 10851891007305 - Arisure | 2025-05-22 Arisure Bag Spike |
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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 |