ViaLok

Primary DI
00851891007070
Brand
ViaLok
Company
YUKON MEDICAL, LLC
Model
YM011
Catalog number
YM011
Device description
13mm ViaLok V Vented Vial Access Device
Published
2016-09-23
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
LHISet, I.V. Fluid Transfer

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LHISet, I.V. Fluid TransferGeneral Hospital2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10851891007077PackageGS116In Commercial Distribution
20851891007074PackageGS125In Commercial Distribution
50851891007075PackageGS1100In Commercial Distribution
00851891007070PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1085189100707710851891007077
2085189100707420851891007074
5085189100707550851891007075
00851891007070008518910070708518910070700851891007070

GMDN Terms#

Term, Definition table
TermDefinition
Vial/bottle adaptor, non-hermeticA device intended to be fitted to a vial or bottle to enable the removal of its contents, (e.g., medication, nutritional solution for enteral feeding) into a syringe, for subsequent administration to a patient. It is typically a housing with a barbed connection or spike that attaches to or replaces the container lid, and a small bore connection (typically ENFit or a Luer); it does not allow for pressure equalization/airtight transfer of contents. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Lumen/Inner Diameter0

Contacts#

Phone, Email table
PhoneEmail
919-595-8250Quality@YukonMedical.com

Regulatory Flags#

DUNS number
963361170
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
true
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00851891007292ArisureYM060YM0602025-05-14
00851891007605ArisureYM060YM0602025-06-30
20851891007609ArisureYM060YM0602025-06-30
00851891007629ArisureYM062YM0622025-05-23
20851891007623ArisureYM062YM0622025-05-23
00851891007308ArisureYM061YM0612025-05-14
10851891007299ArisureYM060YM0602025-05-14
10851891007305ArisureYM061YM0612025-05-14
00851891007360ArisureYM104-05YM104-052024-12-03
00851891007322ArisureYM106YM1062024-11-27
00851891007353ArisureYM107YM1072024-11-27
10851891007329ArisureYM106YM1062024-11-27
10851891007350ArisureYM107YM1072024-11-27
10885403228100SmartSiteMV0513MV05132017-04-03
10885403228445SmartSiteMV0413MV04132017-02-07
10885403228452SmartSiteMV0420MV04202016-09-22
10885403228469SmartSiteMV0428MV04282017-04-06
10885403229022SmartSiteMV0528MV05282017-04-06
10885403232664NoneMV0620MV06202017-07-10
10885403232671NoneMV0613MV06132017-07-07

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