Primary Device ID | 50851891007167 |
NIH Device Record Key | ababa33e-447d-41ba-9758-b09795c1ee8a |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | YM004 |
Catalog Number | YM004 |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00851891007162 [Primary] |
GS1 | 50851891007167 [Package] Contains: 00851891007162 Package: Case [100 Units] In Commercial Distribution |
FPA | Set, Administration, Intravascular |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-03-27 |
Device Publish Date | 2023-03-17 |
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 |
20885403228466 - SmartSite | 2023-05-18 SMARTSITE 28MM VENTED VIAL ACCESS DEVICE |
50885403229020 - SmartSite | 2023-05-18 SMARTSITE VIALSHIELD 28MM CLOSED VAD |
50885403232662 - None | 2023-05-18 MALE LUER 20MM VIAL ACCESS DEVICE |