Fluid Management Set 194209

GUDID 20886333207644

Fluid Management Set

ARGON MEDICAL DEVICES, INC.

Fluid transfer set, general-purpose
Primary Device ID20886333207644
NIH Device Record Keydd7794cd-ff2c-4ccb-b047-bf054e8570c5
Commercial Distribution StatusIn Commercial Distribution
Brand NameFluid Management Set
Version Model Number194209
Catalog Number194209
Company DUNS140727624
Company NameARGON MEDICAL DEVICES, INC.
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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100886333207640 [Primary]
GS120886333207644 [Package]
Contains: 00886333207640
Package: Box [20 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DXTInjector And Syringe, Angiographic

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2016-09-15

Devices Manufactured by ARGON MEDICAL DEVICES, INC.

20886333227864 - V-Stick Vascular Access Set2026-03-30 V-Stick™ Vascular Access Set 4F with Talwire
20886333227871 - V-Stick Vascular Access Set2026-03-30 V-Stick Vascular Access Set 5F with Talwire
20886333227888 - V-Stick Vascular Access Set 2026-03-30 V-Stick Vascular Access Set 5F with Talwire
20886333227895 - V-Stick Vascular Access Set2026-03-30 V-Stick Vascular Access Set 4F with Talwire
20886333227901 - V-Stick Vascular Access Set 2026-03-30 V-Stick Vascular Access Set 5F with Talwire
20886333227918 - V- Stick Vascular Access Set2026-03-30 V- Stick Vascular Access Set 5F with Talwire
20886333227925 - V-Stick Vascular Access Set2026-03-30 V-Stick Vascular Access Set 4F with Talwire
20886333227932 - V-Stick Vascular Access Set2026-03-30 V-Stick Vascular Access Set 4F with Talwire

© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.