ACIST CVi® Angiographic Injection System Control Panel

GUDID 10841716101196

CVi Angiographic Injection System Control Panel, p/n 701557-001

ACIST MEDICAL SYSTEMS, INC.

Angiography contrast medium injection system, line-powered, mobile

• Primary Device ID: 10841716101196
• NIH Device Record Key: 56382e72-bf59-4f1b-a26f-9fd33303c732
• Commercial Distribution Discontinuation: 2018-06-13
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: ACIST CVi® Angiographic Injection System Control Panel
• Version Model Number: 017738
• 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	10841716101196 [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 Control Panel]

• 30841716100629: CVi Angiographic Injection System Control Panel, p/n 700771-005
• 10841716101196: CVi Angiographic Injection System Control Panel, p/n 701557-001