EASYSCOPE

GUDID 08031527014913

MICROPORT CRM SRL

Electrocardiographic long-term ambulatory recording analyser

• Primary Device ID: 08031527014913
• NIH Device Record Key: 964ec742-8305-4548-8a04-a2a97e4a8df0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EASYSCOPE
• Version Model Number: V3.10 Network Lic.USB
• Company DUNS: 438860859
• Company Name: MICROPORT CRM SRL
• 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: false
• 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	08031527014913 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K042002

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: 4
• Public Version Date: 2020-10-20
• Device Publish Date: 2016-09-22

On-Brand Devices [EASYSCOPE]

• 08031527014944: V3.10 UPG TO USB COM
• 08031527014913: V3.10 Network Lic.USB
• 08031527014296: V3.10 USB COM