Vessel Clude 046-1-130A

GUDID 20886333222708

Vessel Clude Large

ARGON MEDICAL DEVICES, INC.

Surgical vessel loop

• Primary Device ID: 20886333222708
• NIH Device Record Key: 226e10de-3cca-49a3-a05f-48a38b9e74de
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vessel Clude
• Version Model Number: 046-1-130A
• Catalog Number: 046-1-130A
• Company DUNS: 140727624
• Company Name: ARGON MEDICAL DEVICES, INC.
• 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: 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

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00886333222704 [Primary]
GS1	20886333222708 [Package]; Contains: 00886333222704; Package: Box [10 Units]; In Commercial Distribution

FDA Product Code

• DXC: Clamp, Vascular

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-05-06
• Device Publish Date: 2016-09-23

On-Brand Devices [Vessel Clude]

• 20886333222708: Vessel Clude Large
• 20886333222685: Vessel Clude Medium
• 20886333222678: Vessel Clude Small