Percutaneous Micro-Introducer Kit 497817

GUDID 10886333215062

5F Percutaneous Micro-Introducer Kit

ARGON MEDICAL DEVICES, INC.

Magnetocardiography system
Primary Device ID10886333215062
NIH Device Record Key449298d8-5d1d-4a7e-a53a-52b0dac3a758
Commercial Distribution StatusIn Commercial Distribution
Brand NamePercutaneous Micro-Introducer Kit
Version Model Number497817
Catalog Number497817
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

Device Dimensions

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Device Identifiers

Device Issuing AgencyDevice ID
GS100886333215065 [Primary]
GS110886333215062 [Package]
Contains: 00886333215065
Package: Box [10 Units]
In Commercial Distribution
GS120886333215069 [Package]
Contains: 00886333215065
Package: Box [50 Units]
In Commercial Distribution

FDA Product Code

OFLPercutaneous Sheath Introducer Kit

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 Date2016-09-09

On-Brand Devices [Percutaneous Micro-Introducer Kit]

10886333215079Percutaneous Micro-Introducer Kit 4F
108863332150625F Percutaneous Micro-Introducer Kit
108863332150554F Percutaneous Micro-Introducer Kit
108863332150485F Percutaneous Micro-Introducer Kit
108863332150314F Percutaneous Micro-Introducer Kit
108863332150245F Percutaneous Micro-Introducer Kit
108863332150174F Percutaneous Micro-Introducer Kit
108863332150005F Percutaneous Micro-Introducer Kit
108863332149974F Percutaneous Micro-Introducer Kit

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