ACIST CVi® Angiographic Injection System Control Panel

GUDID 30841716100629

CVi Angiographic Injection System Control Panel, p/n 700771-005

ACIST MEDICAL SYSTEMS, INC.

Angiography contrast medium injection system, line-powered, mobile

• Primary Device ID: 30841716100629
• NIH Device Record Key: 7dddca59-0213-487c-9b6b-e913e61e42f3
• Commercial Distribution Discontinuation: 2019-02-20
• 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	10841716100625 [Primary]
GS1	30841716100629 [Package]; Contains: 10841716100625; Package: Shelf Box [1 Units]; Discontinued: 2019-02-20; Not in Commercial Distribution

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: 2019-04-15
• Device Publish Date: 2016-09-21

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