Horizon XVu 960-800-315

GUDID 07290102932788

Computerized Hemodynamic monitoring System

MENNEN MEDICAL LTD.

Cardiac catheterization laboratory computer

• Primary Device ID: 07290102932788
• NIH Device Record Key: e5fe5f3a-541c-4760-b5b8-7305fb1e4344
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Horizon XVu
• Version Model Number: Lite_115V
• Catalog Number: 960-800-315
• Company DUNS: 600019749
• Company Name: MENNEN MEDICAL LTD.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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

Customer Support Contacts

• Phone: +2152591020
• Email: info@mmi.co.il

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290102932788 [Primary]

FDA Product Code

• DQK: Computer, Diagnostic, Programmable

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: 2018-03-29
• Device Publish Date: 2016-09-24

On-Brand Devices [Horizon XVu]

• 07290102932788: Computerized Hemodynamic monitoring System
• 07290102932771: Computerized Hemodynamic monitoring System