MAXXWIRE® 80129-406/A

GUDID 00884450458082

Merit Medical Systems, Inc.

Gastro-urological guidewire, single-use

• Primary Device ID: 00884450458082
• NIH Device Record Key: 8eff550f-de3a-47ca-a68a-5e02a3662df9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MAXXWIRE®
• Version Model Number: 10884450458089
• Catalog Number: 80129-406/A
• Company DUNS: 184763290
• Company Name: Merit Medical Systems, Inc.
• Device Count: 2
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884450458082 [Unit of Use]
GS1	10884450458089 [Primary]

FDA Product Code

• MDM: INSTRUMENT, MANUAL, SURGICAL, GENERAL USE

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: 2020-09-03
• Device Publish Date: 2020-08-26

On-Brand Devices [MAXXWIRE®]

• 00884450458082: 10884450458089
• 00884450458075: 10884450458072
• 10884450044954: 10884450044954
• 10884450044947: 10884450044947