Critiflo™ 682060/B

GUDID 20884450371859

ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD.

Invasive blood pressure monitoring flush tubing

• Primary Device ID: 20884450371859
• NIH Device Record Key: 8cc0c1dd-46c4-4d10-9c37-ed1529b029f9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Critiflo™
• Version Model Number: 10884450371852
• Catalog Number: 682060/B
• Company DUNS: 595138793
• Company Name: ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD.
• Device Count: 10
• 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	00884450371855 [Unit of Use]
GS1	10884450371852 [Primary]
GS1	20884450371859 [Package]; Contains: 10884450371852; Package: [10 Units]; In Commercial Distribution

FDA Product Code

• KRA: Catheter, continuous flush

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: 2021-12-13
• Device Publish Date: 2019-07-24

On-Brand Devices [Critiflo™]

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