EMS-XL 965-100-135

GUDID 07290102932818

Cardiac electrophysiology analysis system

MENNEN MEDICAL LTD.

Cardiac electrophysiology analysis system

• Primary Device ID: 07290102932818
• NIH Device Record Key: 7b542b86-bc69-4ea9-9399-971337bea281
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EMS-XL
• Version Model Number: 32 Ch. Lite System
• Catalog Number: 965-100-135
• 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	07290102932818 [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 [EMS-XL]

• 07290102933082: Cardiac electrophysiology analysis system
• 07290102933075: Cardiac electrophysiology analysis system
• 07290102933068: Cardiac electrophysiology analysis system
• 07290102933051: Cardiac electrophysiology analysis system
• 07290102932832: Cardiac electrophysiology analysis system
• 07290102932818: Cardiac electrophysiology analysis system