Midmark 1-100-1550

GUDID 08056732652491

ECG acquisition capabilities to resting ECG and stress test systems. (Wireless acquisition module)

CARDIOLINE SPA

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• Primary Device ID: 08056732652491
• NIH Device Record Key: e9a0d3e3-9eaa-406f-b4ea-4951f35d3db3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Midmark
• Version Model Number: Midmark Digital ECG
• Catalog Number: 1-100-1550
• Company DUNS: 339465174
• Company Name: CARDIOLINE SPA
• 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	08056732652491 [Primary]

FDA Product Code

• DRG: Transmitters And Receivers, Physiological Signal, Radiofrequency

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-12-13
• Device Publish Date: 2023-12-05

Devices Manufactured by CARDIOLINE SPA

• 08056732652491 - Midmark: 2023-12-13ECG acquisition capabilities to resting ECG and stress test systems. (Wireless acquisition module)
• 08056732652491 - Midmark: 2023-12-13 ECG acquisition capabilities to resting ECG and stress test systems. (Wireless acquisition module)
• 08056732653610 - ECG100+: 2021-03-10 12‐lead high‐performance, multi‐channel, interpretative resting electrocardiograph which displays, acquires, prints and st
• 08056732654587 - touchECG: 2021-03-10 Software that implements a multichannel interpretative electrocardiograph designed to check and diagnose cardiac function.