Denali® Vena Cava Filter DL900F

GUDID 00801741040801

DENALI® Vena Cava Filter Femoral

Bard Peripheral Vascular, Inc.

Vena cava filter, temporary/permanent

• Primary Device ID: 00801741040801
• NIH Device Record Key: a4cc6bb4-f747-4ef2-8d37-06262264f1a3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Denali® Vena Cava Filter
• Version Model Number: DL900F
• Catalog Number: DL900F
• Company DUNS: 135057938
• Company Name: Bard Peripheral Vascular, 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: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)321-4254
• Email: medical.services@crbard.com
• Phone: +1(800)321-4254
• Email: medical.services@crbard.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
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry
• Special Storage Condition, Specify: Between 0 and 0 *Keep Dry

Device Identifiers

Device Issuing Agency	Device ID
GS1	00801741040801 [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: 2015-09-24

On-Brand Devices [Denali® Vena Cava Filter]

• 00801741040801: DENALI® Vena Cava Filter Femoral
• 00801741040795: DENALI® Vena Cava Filter Jugular/Subclavian