Manifold Kit 196031

GUDID 20886333208566

Manifold Kit

ARGON MEDICAL DEVICES, INC.

Angiography kit

• Primary Device ID: 20886333208566
• NIH Device Record Key: 3d45b792-4528-42b8-89a8-49c17bffe1c9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Manifold Kit
• Version Model Number: 196031
• Catalog Number: 196031
• 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: true
• 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 Identifiers

Device Issuing Agency	Device ID
GS1	00886333208562 [Primary]
GS1	20886333208566 [Package]; Contains: 00886333208562; Package: Box [10 Units]; In Commercial Distribution

FDA Product Code

• OJA: Intravenous Extension Tubing Set

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: 2016-09-21

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