Crux® Vena Cava FIlter, Jugular

GUDID 00845225002534

VOLCANO CORPORATION

Vena cava filter, temporary/permanent

• Primary Device ID: 00845225002534
• NIH Device Record Key: 50fda220-9cdc-413b-a9b3-17df84c0afbb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Crux® Vena Cava FIlter, Jugular
• Version Model Number: 7025
• Company DUNS: 135179237
• Company Name: VOLCANO CORPORATION
• 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: false
• Serial Number: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00845225002534 [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: 2015-09-17

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