ViaLok YM011

GUDID 50851891007075

13mm Vented Vial Access Device

YUKON MEDICAL, LLC

Vial transfer spike
Primary Device ID50851891007075
NIH Device Record Key9075e128-ea80-41fc-a1c5-e1d925b30f40
Commercial Distribution StatusIn Commercial Distribution
Brand NameViaLok
Version Model NumberYM011
Catalog NumberYM011
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
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 Dimensions

Lumen/Inner Diameter13 Millimeter
Lumen/Inner Diameter13 Millimeter
Lumen/Inner Diameter13 Millimeter
Lumen/Inner Diameter13 Millimeter
Lumen/Inner Diameter13 Millimeter
Lumen/Inner Diameter13 Millimeter
Lumen/Inner Diameter13 Millimeter
Lumen/Inner Diameter13 Millimeter
Lumen/Inner Diameter13 Millimeter
Lumen/Inner Diameter13 Millimeter
Lumen/Inner Diameter13 Millimeter
Lumen/Inner Diameter13 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100851891007070 [Primary]
GS150851891007075 [Package]
Contains: 00851891007070
Package: Case [100 Units]
In Commercial Distribution

FDA Product Code

LHISet, I.V. Fluid Transfer

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2018-03-29
Device Publish Date2016-09-23

On-Brand Devices [ViaLok]

5085189100733413mm Multi-Dose Non-Vented Vial Adapter
0085189100709420mm Vented Vial Access Device
5085189100708220mm Vented Vial Access Device, sm
5085189100707513mm Vented Vial Access Device
5085189100706813 mm Vial Access Device, Male
5085189100705113mm Vial Access Device
5085189100704420mm Vial Access Device
5085189100702028mm Multi-Dose Vented Vial Adapter
5085189100701320mm Multi-Dose Vented Vial Adapter
5085189100700613mm Multi-Dose Vented Vial Adapter
5085189100734120mm Multi-Dose Non-Vented Vial Adapter
5085189100719820mm Male Luer Lock Vial Access Device

Trademark Results [ViaLok]

Mark Image

Registration | Serial
Company
Trademark
Application Date
VIALOK
VIALOK
85328409 4309669 Live/Registered
Yukon Medical, LLC
2011-05-24

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.