Navigator 60-3002

GUDID 10815149025312

Extension cable for use with Navigator

CORPAK MEDSYSTEMS, INC.

Intravascular catheter stylet magnet detector

• Primary Device ID: 10815149025312
• NIH Device Record Key: fcc13a0e-fc5a-4cde-b4c3-157e9d63716b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Navigator
• Version Model Number: 60-3002
• Catalog Number: 60-3002
• Company DUNS: 147530323
• Company Name: CORPAK MEDSYSTEMS, INC.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(847)403-3400
• Email: questions@corpak.com
• Phone: +1(847)403-3400
• Email: questions@corpak.com
• Phone: +1(847)403-3400
• Email: questions@corpak.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10815149025312 [Primary]

FDA Product Code

• FOZ: Catheter,intravascular,therapeutic,short-term less than 30 days

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-05-19
• Device Publish Date: 2016-08-04

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