Percutaneous Micro-Introducer Kit 497814

GUDID 10886333215048

5F Percutaneous Micro-Introducer Kit

ARGON MEDICAL DEVICES, INC.

Magnetocardiography system
Primary Device ID10886333215048
NIH Device Record Keyf5923d9e-a6d3-48d4-b54d-180aca7206a6
Commercial Distribution StatusIn Commercial Distribution
Brand NamePercutaneous Micro-Introducer Kit
Version Model Number497814
Catalog Number497814
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
GS100886333215041 [Primary]
GS110886333215048 [Package]
Contains: 00886333215041
Package: Box [10 Units]
In Commercial Distribution
GS120886333215045 [Package]
Contains: 00886333215041
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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