Thermodilution Catheter 497520

GUDID 20886333214666

Thermodilution Catheter 7.5F - 5 Lumen

ARGON MEDICAL DEVICES, INC.

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• Primary Device ID: 20886333214666
• NIH Device Record Key: 9b7887d1-8455-4b61-8283-33a9e1d18449
• Commercial Distribution Discontinuation: 2017-11-02
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Thermodilution Catheter
• Version Model Number: 497520
• Catalog Number: 497520
• Company DUNS: 140727624
• Company Name: ARGON MEDICAL DEVICES, INC.
• Device Count: 1
• DM Exempt: false
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry and Away from Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry and Away from Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry and Away from Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry and Away from Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry and Away from Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry and Away from Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry and Away from Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry and Away from Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry and Away from Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry and Away from Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry and Away from Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry and Away from Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry and Away from Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry and Away from Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry and Away from Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry and Away from Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry and Away from Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry and Away from Sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry and Away from Sunlight

Device Identifiers

Device Issuing Agency	Device ID
GS1	00886333214662 [Primary]
GS1	20886333214666 [Package]; Contains: 00886333214662; Package: Box [5 Units]; Discontinued: 2017-11-02; Not in Commercial Distribution

FDA Product Code

• DQO: Catheter, Intravascular, Diagnostic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2019-06-07
• Device Publish Date: 2016-09-21

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• 20886333214734: Thermodilution Catheter 7F - 4Lumen - S Curve
• 20886333214727: Thermodilution Catheter 7F - 4Lumen - S Curve
• 20886333214710: Thermodilution Catheter 7.5F - 5 Lumen - Soft Body
• 20886333214697: Thermodilution Catheter 7F - 4 Lumen - 110cm
• 20886333214673: Thermodilution Catheter 7F - 4Lumen
• 20886333214666: Thermodilution Catheter 7.5F - 5 Lumen