ACIST CVi® Angiographic Injection System Injector Head

GUDID 10841716101349

CVi Injector (Siemens), p/n 700708-009

ACIST MEDICAL SYSTEMS, INC.

Angiography contrast medium injection system, line-powered, mobile

• Primary Device ID: 10841716101349
• NIH Device Record Key: 32bbfb5a-c6dd-4480-b335-43900b5c8b35
• Commercial Distribution Discontinuation: 2018-06-13
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: ACIST CVi® Angiographic Injection System Injector Head
• Version Model Number: 014658
• Company DUNS: 926684994
• Company Name: ACIST MEDICAL SYSTEMS, 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: false
• Device Combination Product: false
• 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	10841716101349 [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: 3
• Public Version Date: 2024-05-17
• Device Publish Date: 2016-09-09

On-Brand Devices [ACIST CVi® Angiographic Injection System Injector Head]

• 10841716100618: CVi Injector (Siemens), p/n 700708-008
• 10841716100601: CVi Injector, p/n 700706-008
• 10841716101349: CVi Injector (Siemens), p/n 700708-009
• 10841716101233: CVi Injector, p/n 700706-009