Certification guides
Massager Compliance Document Guides for Buyers
Supporting documents answer different questions. These buyer guides explain how to distinguish a product certificate, a test report, a component file and an intellectual-property record when reviewing a massage-device proposal. A file applies only to its named model, sample and standard; it is not a whole-range or whole-market approval, and the guides show how to read that scope before an order.
Keep the file with the named model.
Review the published document library and its exact scope, then prepare the questions relevant to your product and destination.
Review model documents01 Europe & UK
Read the applicable scope.
Read the applicable scope. Match the product and cited CE, EMC or RoHS requirements to the original evidence for the exact model; a file title alone does not establish approval for another version or market.
02 United States
Separate the regulatory questions.
Separate the regulatory questions. FCC reports, product safety and any medical-device question are distinct; review the named product, intended use and evidence with the appropriate specialist for the proposed market.
03 Asia & Saudi Arabia
Check the destination requirements.
Check the destination requirements. Use the destination-specific guides to prepare questions about the exact model and ordered version, including which files exist today and which would need new testing.
04 Testing & transport
Connect the file to the order.
Connect the file to the order. Identify whether evidence covers the device or its battery, retain its exact subject and sample scope, and confirm transport documents for lithium batteries before shipment.
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