Navigator 60-3002

GUDID 10815149025312

Extension cable for use with Navigator

CORPAK MEDSYSTEMS, INC.

Intravascular catheter stylet magnet detector Intravascular catheter stylet magnet detector
Primary Device ID10815149025312
NIH Device Record Keyfcc13a0e-fc5a-4cde-b4c3-157e9d63716b
Commercial Distribution StatusIn Commercial Distribution
Brand NameNavigator
Version Model Number60-3002
Catalog Number60-3002
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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
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

Device Identifiers

Device Issuing AgencyDevice ID
GS110815149025312 [Primary]
GS110815149025312 [Primary]

FDA Product Code

FOZCatheter,intravascular,therapeutic,short-term less than 30 days
FOZCatheter,intravascular,therapeutic,short-term less than 30 days

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2020-05-19
Device Publish Date2016-08-04

Devices Manufactured by CORPAK MEDSYSTEMS, INC.

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