FDA.reportPublic FDA data

Percutaneous Micro-Introducer Kit

Primary DI
10886333215048
Brand
Percutaneous Micro-Introducer Kit
Company
ARGON MEDICAL DEVICES, INC.
Model
497814
Catalog number
497814
Device description
5F Percutaneous Micro-Introducer Kit
Published
2016-09-09
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
OFLPercutaneous Sheath Introducer Kit

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
OFLPercutaneous Sheath Introducer KitCardiovascular2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10886333215048PackageGS110In Commercial Distribution
20886333215045PackageGS150In Commercial Distribution
00886333215041PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1088633321504810886333215048
2088633321504520886333215045
00886333215041008863332150418863332150410886333215041

GMDN Terms#

Term, Definition table
TermDefinition
Magnetocardiography systemAn assembly of devices used to non-invasively detect, measure, and display bio-magnetic signals produced by electrically-active neural tissue of the heart that provide diagnostic information about cardiac electrophysiology (EP) [magnetocardiography (MCG)]. It typically consists of a fixed or moveable gantry, a patient table, a dewar [vessel containing liquid helium (He)], dedicated software, and a superconducting quantum interference device (SQUID) sensor array that measures the magnetic fields created by electrical current flowing with neurons. It may be sited within a magnetically-shielded room (MSR), and is used for cardiac mapping and the diagnosis of heart disorders.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Device Size Text, specify0

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
1.800.927.4669Customer.Service@argonmedical.com

Regulatory Flags#

DUNS number
140727624
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
true
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

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00886333006199Skater Nephrostomy Catheter7556100357556100352026-10-07
00886333006205Skater All-Purpose Drainage Catheter7560060207560060202026-10-07
00886333006212Skater All-Purpose Drainage Catheter7560070207560070202026-10-07
00886333006229Skater All-Purpose Drainage Catheter7560120257560120252026-10-07
00886333006236Skater All-Purpose Drainage Catheter7560100257560100252026-10-07
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00886333006250Skater All-Purpose Drainage Catheter7565140257565140252026-10-07
00886333006267Skater All-Purpose Drainage Catheter7565160257565160252026-10-07
00886333006274Skater All-Purpose Drainage Catheter7565120257565120252026-10-07
00886333006281Skater All-Purpose Drainage Catheter7565100307565100302026-10-07
00886333006298Skater All-Purpose Drainage Catheter7565100257565100252026-10-07
00886333006304Skater All-Purpose Drainage Catheter7565080307565080302026-10-07
00886333006311Skater All-Purpose Drainage Catheter7565080257565080252026-10-07
00886333006328Skater All-Purpose Drainage Catheter7565070257565070252026-10-07
00886333006335Skater All-Purpose Drainage Catheter7565060207565060202026-10-07

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H965459180Navilyst MedicalAngiodynamics, Inc.OFL2024-10-21
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00810050853774Typenex Introducer SetTYPENEX MEDICAL LLCOFL2021-08-11
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