ACIST HDi® Power Supply

GUDID 30841716101176

HDi Power Supply, p/n 701560-002

ACIST MEDICAL SYSTEMS, INC.

Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system Cardiovascular ultrasound imaging system

• Primary Device ID: 30841716101176
• NIH Device Record Key: 448c6f42-9a7d-4f60-830c-7b993906e194
• Commercial Distribution Discontinuation: 2020-01-14
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: ACIST HDi® Power Supply
• Version Model Number: 017990
• 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	10841716101172 [Primary]
GS1	30841716101176 [Package]; Contains: 10841716101172; Package: Shelf box [1 Units]; Discontinued: 2020-01-14; Not in Commercial Distribution

FDA Product Code

• OBJ: Catheter, Ultrasound, Intravascular

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: 2024-05-09
• Device Publish Date: 2016-09-09

Devices Manufactured by ACIST MEDICAL SYSTEMS, INC.

• 30841716100070 - ACIST CVi® Cart: 2024-05-31 CVi Cart, p/n 701351-001
• 30841716102616 - Single-use Syringe Kit: 2024-05-29 Model A1000V, p/n 701259-012 Kit Contents: 100mL contrast reservoir and tubing with contrast spike and clamp
• 30841716102609 - A1000 Single Use Syringe Kit: 2024-05-27 A1000 Single Use Syringe Kit, p/n 701669-009 Kit Contents: 100mL contrast reservoir and tubing with contrast spike and clamp.
• 10841716100632 - ACIST CVi® Angiographic Injection System Power Supply: 2024-05-17 CVi Power Supply p/n 701340-002
• 10841716101196 - ACIST CVi® Angiographic Injection System Control Panel: 2024-05-17 CVi Angiographic Injection System Control Panel, p/n 701557-001
• 10841716101233 - ACIST CVi® Angiographic Injection System Injector Head: 2024-05-17 CVi Injector, p/n 700706-009
• 10841716101349 - ACIST CVi® Angiographic Injection System Injector Head: 2024-05-17 CVi Injector (Siemens), p/n 700708-009
• 30841716102548 - A2000 Multi-use Syringe Kit: 2024-05-17 A2000 Multi-use Syringe Kit, p/n 701669-008 Kit Contents: 100mL contrast reservoir and tubing with contrast spike and clamp with