Registration Requirements
All medical devices sold must comply with local regulations (MOH / SFDA / DHA).
- Import License: Items manufactured outside the country must have valid import permits.
- AR (Authorized Representative): Vendors must be authorized agents for the brands they sell.
Prohibited Actions
- Selling devices with expired calibration.
- Selling "Professional Use Only" devices to home users without verifying credentials.
Recall Protocol
In the event of a manufacturer recall:
- Vendor must notify Phyzioline Compliance Team immediately (within 4 hours).
- Phyzioline will freeze all inventory and notify affected customers.
- Vendor bears all costs for reverse logistics and replacements.