Sourcing guide
FCC Documents for Electronic Massagers
FCC-related records are published for F101 and F12 under 47 CFR Part 15 Subpart B.
More context
F101 uses reference WTH26H05139795E; F12 uses WTH25H12332361E. Both have named report records. These concern their stated emissions scope, rather than universal US product safety or medical approval.
Meilan F101 Foldable Neck Massager View model details Products and selection
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Buyer facts
Facts to compare
| Named product or component | Reference number | File | Original path | Stated standards |
|---|---|---|---|---|
| F101 | WTH26H05139795E | F101 FCC Verification Document | /documents/certifications/f101-fcc.pdf | 47 CFR Part 15 Subpart B |
| F101 | WTH26H05139795E | F101 FCC Test Report | /documents/certifications/f101-fcc-report.pdf | 47 CFR Part 15 Subpart B |
| F12 | WTH25H12332361E | F12 FCC Verification Document | /documents/certifications/f12-fcc.pdf | 47 CFR Part 15 Subpart B |
| F12 | WTH25H12332361E | F12 FCC Test Report | /documents/certifications/f12-fcc-report.pdf | 47 CFR Part 15 Subpart B |
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Before you order
Official framework and original files
- Official guidance
https://www.fcc.gov/oet/ea/rfdevice
- Original evidence
F101 FCC Verification Document: /documents/certifications/f101-fcc.pdf | F101 FCC Test Report: /documents/certifications/f101-fcc-report.pdf | F12 FCC Verification Document: /documents/certifications/f12-fcc.pdf | F12 FCC Test Report: /documents/certifications/f12-fcc-report.pdf
Buyer guide
Selection guide
What do the F101 and F12 FCC files show?
The available FCC files concern the named electronic products and the rule part printed in the originals. F101 reference WTH26H05139795E and F12 reference WTH25H12332361E identify separate assessments under 47 CFR Part 15 Subpart B. The corresponding reports record Pass for the tested samples. This is useful emissions evidence for those configurations; it is not a blanket statement that every Meilan model has completed every US regulatory obligation. FCC rules address radio-frequency equipment, and the applicable authorization route depends on the equipment design. A document called a certificate by a laboratory is not automatically an FCC grant of authorization. Its actual content and regulatory route establish what it means.
Does a Bluetooth option use the same evidence?
A wireless option can introduce a different regulatory question from the non-transmitter emissions assessment shown in a Part 15 Subpart B file. The radio module, antenna, host integration and operating configuration matter to the final route. Accordingly, a Bluetooth marketing label and a named FCC emissions report are not interchangeable evidence. The F101 and F12 records shown here remain tied to their stated models and scope; no separate transmitter authorization is inferred from them. For a private-label project, the complete supplied electronics and accessories determine how existing evidence relates to the final product. A cosmetic logo change is different from a module replacement or new radio function.
Purchasing FAQ
Common buying questions
Which US rule part appears in the published files?
47 CFR Part 15 Subpart B appears in the F101 and F12 records.
Do these files establish medical approval?
No. FCC-related emissions evidence does not establish a medical intended use or FDA status.
Is every Bluetooth configuration covered?
No universal radio-configuration coverage is established by the displayed Subpart B records.
Are F12 and F101 under one reference?
No. Their references are WTH25H12332361E and WTH26H05139795E respectively.
What do the F101 and F12 FCC files show?
The available FCC files concern the named electronic products and the rule part printed in the originals. F101 reference WTH26H05139795E and F12 reference WTH25H12332361E identify separate assessments under 47 CFR Part 15 Subpart B.
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