YM004

GUDID 50851891007167

Neutral Valve

YUKON MEDICAL, LLC

Neutral-pressure intravenous line needleless valve-connector
Primary Device ID50851891007167
NIH Device Record Keyababa33e-447d-41ba-9758-b09795c1ee8a
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberYM004
Catalog NumberYM004
Company DUNS963361170
Company NameYUKON MEDICAL, LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone919-595-8250
EmailQuality@YukonMedical.com
Phone919-595-8250
EmailQuality@YukonMedical.com
Phone919-595-8250
EmailQuality@YukonMedical.com
Phone919-595-8250
EmailQuality@YukonMedical.com
Phone919-595-8250
EmailQuality@YukonMedical.com
Phone919-595-8250
EmailQuality@YukonMedical.com
Phone919-595-8250
EmailQuality@YukonMedical.com
Phone919-595-8250
EmailQuality@YukonMedical.com
Phone919-595-8250
EmailQuality@YukonMedical.com
Phone919-595-8250
EmailQuality@YukonMedical.com
Phone919-595-8250
EmailQuality@YukonMedical.com
Phone919-595-8250
EmailQuality@YukonMedical.com
Phone919-595-8250
EmailQuality@YukonMedical.com
Phone919-595-8250
EmailQuality@YukonMedical.com
Phone919-595-8250
EmailQuality@YukonMedical.com
Phone919-595-8250
EmailQuality@YukonMedical.com
Phone919-595-8250
EmailQuality@YukonMedical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100851891007162 [Primary]
GS150851891007167 [Package]
Contains: 00851891007162
Package: Case [100 Units]
In Commercial Distribution

FDA Product Code

FPASet, Administration, Intravascular

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-03-27
Device Publish Date2023-03-17

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