Option Elite Retrievable Vena Cava Filter System 352506070E

GUDID 00886333217151

Option Elite Retrievable Vena Cava Filter Suitable for Jugular or Femoral Delivery

ARGON MEDICAL DEVICES, INC.

Vena cava filter, temporary/permanent Vena cava filter, temporary/permanent

• Primary Device ID: 00886333217151
• NIH Device Record Key: c3e88230-99d8-4e1f-9fc7-de4d9496b54d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Option Elite Retrievable Vena Cava Filter System
• Version Model Number: 352506070E
• Catalog Number: 352506070E
• Company DUNS: 140727624
• Company Name: ARGON MEDICAL DEVICES, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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: false
• 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

Device Dimensions

• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00886333217151 [Primary]

FDA Product Code

• DTK: Filter, Intravascular, Cardiovascular

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-21

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