Mapcath stylet 60-2018

GUDID 20815149025272

stylet for use with Navigator

CORPAK MEDSYSTEMS, INC.

Intravascular catheter stylet magnet detector Intravascular catheter stylet magnet detector Intravascular catheter stylet magnet detector Intravascular catheter stylet magnet detector Intravascular catheter stylet magnet detector Intravascular catheter stylet magnet detector Intravascular catheter stylet magnet detector Intravascular catheter stylet magnet detector Intravascular catheter stylet magnet detector Intravascular catheter stylet magnet detector Intravascular catheter stylet magnet detector Intravascular catheter stylet magnet detector Intravascular catheter stylet magnet detector Intravascular catheter stylet magnet detector Intravascular catheter stylet magnet detector Intravascular catheter stylet magnet detector
Primary Device ID20815149025272
NIH Device Record Key3a27ee05-81c2-4d79-9534-4ff3be9dbc18
Commercial Distribution Discontinuation2021-01-22
Commercial Distribution StatusNot in Commercial Distribution
Brand NameMapcath stylet
Version Model Number60-2018
Catalog Number60-2018
Company DUNS147530323
Company NameCORPAK MEDSYSTEMS, INC.
Device Count1
DM Exempttrue
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com
Phone+1(847)403-3400
Emailquestions@corpak.com

Device Dimensions

Catheter Gauge1.1 French
Device Size Text, specify0
Length106 Centimeter
Catheter Gauge1.1 French
Device Size Text, specify0
Length106 Centimeter
Catheter Gauge1.1 French
Device Size Text, specify0
Length106 Centimeter
Catheter Gauge1.1 French
Device Size Text, specify0
Length106 Centimeter
Catheter Gauge1.1 French
Device Size Text, specify0
Length106 Centimeter
Catheter Gauge1.1 French
Device Size Text, specify0
Length106 Centimeter
Catheter Gauge1.1 French
Device Size Text, specify0
Length106 Centimeter
Catheter Gauge1.1 French
Device Size Text, specify0
Length106 Centimeter
Catheter Gauge1.1 French
Device Size Text, specify0
Length106 Centimeter
Catheter Gauge1.1 French
Device Size Text, specify0
Length106 Centimeter
Catheter Gauge1.1 French
Device Size Text, specify0
Length106 Centimeter
Catheter Gauge1.1 French
Device Size Text, specify0
Length106 Centimeter
Catheter Gauge1.1 French
Device Size Text, specify0
Length106 Centimeter
Catheter Gauge1.1 French
Device Size Text, specify0
Length106 Centimeter
Catheter Gauge1.1 French
Device Size Text, specify0
Length106 Centimeter
Catheter Gauge1.1 French
Device Size Text, specify0
Length106 Centimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS110815149025275 [Primary]
GS120815149025272 [Package]
Contains: 10815149025275
Package: [10 Units]
Discontinued: 2021-01-22
Not in Commercial Distribution

FDA Product Code

LJSCatheter,intravascular,therapeutic,long-term greater than 30 days

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[20815149025272]

Radiation Sterilization


[20815149025272]

Radiation Sterilization


[20815149025272]

Radiation Sterilization


[20815149025272]

Radiation Sterilization


[20815149025272]

Radiation Sterilization


[20815149025272]

Radiation Sterilization


[20815149025272]

Radiation Sterilization


[20815149025272]

Radiation Sterilization


[20815149025272]

Radiation Sterilization


[20815149025272]

Radiation Sterilization


[20815149025272]

Radiation Sterilization


[20815149025272]

Radiation Sterilization


[20815149025272]

Radiation Sterilization


[20815149025272]

Radiation Sterilization


[20815149025272]

Radiation Sterilization


[20815149025272]

Radiation Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2023-07-31
Device Publish Date2016-08-04

On-Brand Devices [Mapcath stylet]

20815149025272stylet for use with Navigator
20815149025265stylet for use with Navigator

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