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Statement of InformationSingle residential property located in the Melbourne
metropolitan area
Section 47AF of the Estate Agents Act 1980
Property offered for sale
Address
Including suburb and
postcode9
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What is coldstream device database?
The Coldstream Device Database is a centralized repository for tracking and managing medical devices, ensuring compliance with safety and regulatory standards.
Who is required to file coldstream device database?
Manufacturers and distributors of medical devices are required to file the Coldstream Device Database.
How to fill out coldstream device database?
To fill out the Coldstream Device Database, users must provide information about the device, its intended use, manufacturing details, and compliance with regulations.
What is the purpose of coldstream device database?
The purpose of the Coldstream Device Database is to enhance the safety and oversight of medical devices through improved tracking and reporting.
What information must be reported on coldstream device database?
Information that must be reported includes device identification, manufacturer details, usage data, and any reported incidents or malfunctions.
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