Primary Device ID | 40851891007122 |
NIH Device Record Key | 1487a68f-257b-4b81-8e23-be1b3561d5d9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Arisure |
Version Model Number | YM050 |
Catalog Number | YM050 |
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 | 00851891007124 [Primary] |
GS1 | 10851891007121 [Package] Contains: 00851891007124 Package: Dispenser [25 Units] In Commercial Distribution |
GS1 | 40851891007122 [Package] Contains: 10851891007121 Package: Case [2 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 |
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 |
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 |