Acumen IQ Fluid Meter AIQFM

GUDID 00690103205817

Acumen IQ Fluid Meter

Edwards Lifesciences LLC

Intravenous line sensor, gravity infusion

• Primary Device ID: 00690103205817
• NIH Device Record Key: 9f29f532-4113-432f-bd00-73bbc8a1ac08
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Acumen IQ Fluid Meter
• Version Model Number: AIQFM
• Catalog Number: AIQFM
• Company DUNS: 134139174
• Company Name: Edwards Lifesciences LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• 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)822-9637
• Email: tech_support@edwards.com
• Phone: +1(800)822-9637
• Email: tech_support@edwards.com
• Phone: +1(800)822-9637
• Email: tech_support@edwards.com
• Phone: +1(800)822-9637
• Email: tech_support@edwards.com
• Phone: +1(800)822-9637
• Email: tech_support@edwards.com
• Phone: +1(800)822-9637
• Email: tech_support@edwards.com
• Phone: +1(800)822-9637
• Email: tech_support@edwards.com
• Phone: +1(800)822-9637
• Email: tech_support@edwards.com
• Phone: +1(800)822-9637
• Email: tech_support@edwards.com
• Phone: +1(800)822-9637
• Email: tech_support@edwards.com
• Phone: +1(800)822-9637
• Email: tech_support@edwards.com
• Phone: +1(800)822-9637
• Email: tech_support@edwards.com
• Phone: +1(800)822-9637
• Email: tech_support@edwards.com
• Phone: +1(800)822-9637
• Email: tech_support@edwards.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, dry place.
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, dry place.
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, dry place.
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, dry place.
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, dry place.
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, dry place.
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, dry place.
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, dry place.
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, dry place.
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, dry place.
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, dry place.
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, dry place.
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, dry place.
• Special Storage Condition, Specify: Between 0 and 0 *Store in a cool, dry place.

Device Identifiers

Device Issuing Agency	Device ID
GS1	00690103205817 [Primary]

FDA Product Code

• DQK: Computer, Diagnostic, Programmable

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-07-18
• Device Publish Date: 2025-07-10

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• 00690103019285 - HEART VALVE SIZER ACCESSORY: 2026-02-19 CARPENTIER-EDWARDS AORTIC OBTURATOR
• 00690103019292 - HEART VALVE SIZER ACCESSORY: 2026-02-19 CARPENTIER-EDWARDS AORTIC OBTURATOR
• 00690103174755 - HEART VALVE SIZER ACCESSORY: 2026-02-19 PERIMOUNT MAGNA SIZER
• 00690103174762 - HEART VALVE SIZER ACCESSORY: 2026-02-19 PERIMOUNT MAGNA SIZER
• 00690103174779 - HEART VALVE SIZER ACCESSORY: 2026-02-19 PERIMOUNT MAGNA SIZER
• 00690103174786 - HEART VALVE SIZER ACCESSORY: 2026-02-19 PERIMOUNT MAGNA SIZER
• 00690103174793 - HEART VALVE SIZER ACCESSORY: 2026-02-19 PERIMOUNT MAGNA SIZER