Critiflo™ 687787/A

GUDID 20884450323902

ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD.

Invasive blood pressure monitoring tubing set

• Primary Device ID: 20884450323902
• NIH Device Record Key: 8ba6fcc5-a809-49e8-a166-3934fb592097
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Critiflo™
• Version Model Number: 10884450323905
• Catalog Number: 687787/A
• Company DUNS: 595138793
• Company Name: ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD.
• Device Count: 15
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884450323908 [Unit of Use]
GS1	10884450323905 [Primary]
GS1	20884450323902 [Package]; Contains: 10884450323905; Package: [5 Units]; In Commercial Distribution

FDA Product Code

• DXN: SYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE

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: 2021-12-13
• Device Publish Date: 2018-01-30

On-Brand Devices [Critiflo™]

• 20884450323162: 10884450323165
• 20884450371859: 10884450371852
• 20884450323902: 10884450323905