Monitoring Kit 042920006D

GUDID 20886333202007

Monitoring Kit

ARGON MEDICAL DEVICES, INC.

Invasive blood pressure transducer set

• Primary Device ID: 20886333202007
• NIH Device Record Key: f64f0e1a-03cc-4326-884a-41bf5e532d41
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Monitoring Kit
• Version Model Number: 042920006D
• Catalog Number: 042920006D
• 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: 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	00886333202003 [Primary]
GS1	20886333202007 [Package]; Contains: 00886333202003; Package: Box [5 Units]; In Commercial Distribution

FDA Product Code

• DRS: Transducer, Blood-Pressure, Extravascular

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: 2019-01-23
• Device Publish Date: 2016-09-16

On-Brand Devices [Monitoring Kit]

• 20886333202007: Monitoring Kit
• 20886333201888: Monitoring Kit - St Louis University