ACIST CVi® Contrast Delivery System Injector Head

GUDID 10841716101882

CVi Injector (Siemens), p/n 700708-010

ACIST MEDICAL SYSTEMS, INC.

Angiography contrast medium injection system, line-powered, mobile

• Primary Device ID: 10841716101882
• NIH Device Record Key: 0a936283-304d-43d7-b77a-a7b403b3ce4d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ACIST CVi® Contrast Delivery System Injector Head
• Version Model Number: 016225
• Company DUNS: 926684994
• Company Name: ACIST MEDICAL SYSTEMS, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: true
• Single Use: false
• Lot Batch: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	10841716101882 [Primary]

FDA Product Code

• DXT: Injector And Syringe, Angiographic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2025-12-08
• Device Publish Date: 2018-06-13

On-Brand Devices [ACIST CVi® Contrast Delivery System Injector Head]

• 10841716101882: CVi Injector (Siemens), p/n 700708-010
• 10841716101875: CVi Injector, p/n 700706-010