Manifold Kit 196050A

GUDID 20886333208610

Manifold Kit

ARGON MEDICAL DEVICES, INC.

Angiography kit Angiography kit Angiography kit Angiography kit Angiography kit Angiography kit Angiography kit Angiography kit Angiography kit Angiography kit Angiography kit Angiography kit Angiography kit Angiography kit Angiography kit Angiography kit Angiography kit Angiography kit Angiography kit Angiography kit
Primary Device ID20886333208610
NIH Device Record Key084ba8ee-253d-4dc8-a9f1-387ea1827ef8
Commercial Distribution StatusIn Commercial Distribution
Brand NameManifold Kit
Version Model Number196050A
Catalog Number196050A
Company DUNS140727624
Company NameARGON MEDICAL DEVICES, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
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
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com
Phone1.800.927.4669
EmailCustomer.Service@argonmedical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100886333208616 [Primary]
GS120886333208610 [Package]
Contains: 00886333208616
Package: Box [10 Units]
In Commercial Distribution

FDA Product Code

OJAIntravenous Extension Tubing Set

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 Date2016-09-15

On-Brand Devices [Manifold Kit]

20886333222920Manifold Kit
20886333222371Manifold Kit
208863332212063 Port Manifold Kit
20886333209334Manifold Kit
20886333209310Manifold Kit
20886333208962Manifold Kit
20886333208634Manifold Kit
20886333208610Manifold Kit
20886333208597Manifold Kit
20886333208573Manifold Kit
20886333208566Manifold Kit
20886333208269Manifold Kit
20886333208245Manifold Kit
20886333208221Manifold Kit
20886333208214Manifold Kit
20886333208207Manifold Kit
20886333208184Manifold Kit
20886333208153Manifold Kit
20886333208122Manifold Kit
20886333207927Manifold Kit
20886333207743Manifold Kit
20886333207637Manifold Kit

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