Arisure YM064
GUDID 10851891007206
Dry Spike Non-Vented
YUKON MEDICAL, LLC
Intravenous fluid bag spike Non-ISO80369 formatted bag access spike Non-ISO80369 formatted bag access spike Non-ISO80369 formatted bag access spike Non-ISO80369 formatted bag access spike Non-ISO80369 formatted bag access spike Non-ISO80369 formatted bag access spike Non-ISO80369 formatted bag access spike Non-ISO80369 formatted bag access spike Non-ISO80369 formatted bag access spike Non-ISO80369 formatted bag access spike Non-ISO80369 formatted bag access spike Non-ISO80369 formatted bag access spike Non-ISO80369 formatted bag access spike Non-ISO80369 formatted bag access spike Non-ISO80369 formatted bag access spike Non-ISO80369 formatted bag access spike Non-ISO80369 formatted bag access spike Non-ISO80369 formatted bag access spike Non-ISO80369 formatted bag access spike Non-ISO80369 formatted bag access spike Non-ISO80369 formatted bag access spike Non-ISO80369 formatted bag access spike Non-ISO80369 formatted bag access spike Non-ISO80369 formatted bag access spike Non-ISO80369 formatted bag access spike Non-ISO80369 formatted bag access spike Non-ISO80369 formatted bag access spike Non-ISO80369 formatted bag access spike Non-ISO80369 formatted bag access spike| Primary Device ID | 10851891007206 |
| NIH Device Record Key | 50c92cb6-a58a-4578-843a-5a02d5e6fbdc |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Arisure |
| Version Model Number | YM064 |
| Catalog Number | YM064 |
| 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 |
Customer Support Contacts
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00851891007209 [Primary] |
| GS1 | 10851891007206 [Package] Contains: 00851891007209 Package: Dispenser [25 Units] In Commercial Distribution |
| GS1 | 20851891007203 [Package] Package: Case [2 Units] In Commercial Distribution |
FDA Product Code
| LHI | Set, I.V. Fluid Transfer |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-06-03 |
| Device Publish Date | 2019-05-24 |
On-Brand Devices [Arisure]
| 50851891007181 | Closed Male Luer with Cap |
| 40851891007153 | 28mm Closed Vial Adapter |
| 40851891007146 | 20mm Closed Vial Adapter |
| 40851891007139 | 13mm Closed Vial Adapter |
| 40851891007122 | Infusion Access Devise |
| 50851891007112 | Closed Male Luer |
| 10851891007206 | Dry Spike Non-Vented |
| 10851891007275 | Closed Male Luer |
| 10851891007268 | 13mm Closed Vial Adapter |
| 10851891007244 | 20mm Closed Vial Adapter HC |
Trademark Results [Arisure]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ARISURE 87283066 5419441 Live/Registered |
Yukon Medical, LLC 2016-12-28 |
 ARISURE 85328422 not registered Dead/Abandoned |
Yukon Medical, LLC 2011-05-24 |
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