SMARTVIEW

GUDID 08031527016788

MICROPORT CRM SRL

Cardiac pulse generator programmer

• Primary Device ID: 08031527016788
• NIH Device Record Key: 7eec29d9-968e-4a2d-8848-44da72a62b0a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SMARTVIEW
• Version Model Number: 2.52 UG1
• 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: true
• Serial Number: false
• 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	08031527016788 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P980049

FDA Product Code

• NVZ: Pulse generator, permanent, implantable

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: 2017-03-07

On-Brand Devices [SMARTVIEW]

• 08031527017174: 2.56
• 08031527016788: 2.52 UG1
• 08031527016375: 2.50 UG1
• 08031527014487: 2.42UG1
• 08031527013886: 2.40UG1
• 08031527021089: SmartView 3.14 UG1 (US)
• 08031527019932: SmartView Connect App