AVANTI+ 402-611T

GUDID 10705032000772

SI AVANTI+ M/L .035 F11

CORDIS CORPORATION

Haemostasis valve Haemostasis valve Haemostasis valve Haemostasis valve Haemostasis valve Haemostasis valve Haemostasis valve Haemostasis valve Haemostasis valve Haemostasis valve Haemostasis valve Haemostasis valve Haemostasis valve Haemostasis valve Haemostasis valve Haemostasis valve Haemostasis valve

• Primary Device ID: 10705032000772
• NIH Device Record Key: 23b4e834-f375-48f8-9843-aefe449bb906
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AVANTI+
• Version Model Number: 402611T
• Catalog Number: 402-611T
• Company DUNS: 806136177
• Company Name: CORDIS CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	10705032000772 [Primary]
GS1	20705032000779 [Package]; Package: Case [5 Units]; In Commercial Distribution

FDA Product Code

• DRE: DILATOR, VESSEL, FOR PERCUTANEOUS CATHETERIZATION

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-03-05
• Device Publish Date: 2016-08-01

On-Brand Devices [AVANTI+]

• 10705032000772: SI AVANTI+ M/L .035 F11
• 10705032000512: SI AVANTI+ M L .035 F4