Vesselpaws, Blue Maxi 001-1-620

GUDID 20886333222999

Vesselpaws, Blue Maxi

ARGON MEDICAL DEVICES, INC.

Surgical vessel loop Surgical vessel loop

• Primary Device ID: 20886333222999
• NIH Device Record Key: 93c72772-f6af-4cbe-9217-690863d28ec3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vesselpaws, Blue Maxi
• Version Model Number: 001-1-620
• Catalog Number: 001-1-620
• Company DUNS: 140727624
• Company Name: ARGON MEDICAL DEVICES, INC.
• Device Count: 1
• 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: 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	00886333222995 [Primary]
GS1	10886333222992 [Package]; Contains: 00886333222995; Package: Box [10 Units]; In Commercial Distribution
GS1	20886333222999 [Package]; Contains: 00886333222995; Package: Box [100 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: 4
• Public Version Date: 2020-05-06
• Device Publish Date: 2016-09-23

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