Option Elite Retrievable Vena Cava Filter 352506070E

GUDID 00886333217519

Option Elite Retrievable Vena Cava Filter Suitable for Jugular or Femoral Delivery - Sterilized at Sterigenics

ARGON MEDICAL DEVICES, INC.

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

• Primary Device ID: 00886333217519
• NIH Device Record Key: 8efc67f8-79aa-4b10-89b4-3d5487396484
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Option Elite Retrievable Vena Cava Filter
• 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
• 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

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00886333217519 [Primary]

FDA Product Code

• DTK: Filter, Intravascular, Cardiovascular

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-08-05
• Device Publish Date: 2019-07-26

On-Brand Devices [Option Elite Retrievable Vena Cava Filter]

• 00886333222346: Option Elite Retrievable Vena Cava Filter Suitable for Antecubital or Popliteal Delivery
• 00886333217519: Option Elite Retrievable Vena Cava Filter Suitable for Jugular or Femoral Delivery - Sterilized