Whole Body Wave Motion Exercise Device

Complete Specifications & System Overview
  • Manufacturer: Hue Light Co., Ltd.
  • Manufacturing origin: South Korea.
  • Manufacturer reference model: WME-01; U.S. configuration confirmation pending.
  • Category: Wellness exercise equipmentβ€”not a medical device.
  • Environment: Indoor use.

Manufacturer’s WME-01 data

Specification

Length930 mm / approximately 36.6 inches

Width820 mm / approximately 32.3 inches

Height1,660 mm / approximately 65.4 inches

Equipment weight110 kg / approximately 243 lb

FrameHeavy-duty rigid construction

These are equipment dimensions, not required room dimensions. Allow additional space for access, positioning, and any seating.

Maximum user weight, platform dimensions, step-up height, and installation clearances: Obtain from the supplier before approving suitability or placement.

  • Technology: PEMF and sonic motion.
  • U.S. frequency listing: 3–30 Hz.
  • Manufacturer’s WME-01 frequency listing: 5–30 Hz.
  • Intensity: Ten levels, 10–100%.
  • Timer: 1–20 minutes.

Frequency requires confirmation: Do not publish a single definitive range until the U.S. model/version is verified.

Amplitude requires clarification: The manufacturer lists β€œ8–58 mm.” Obtain its measurement definition and corrected technical documentation before using this figure in customer-facing copy.

  • Support handrails.
  • Standing use.
  • Seated use with feet on the platform.

Confirm individual suitability, required supervision, and approved positions using the current operating manual. Handrails do not establish that the device is appropriate for unsupervised use by someone with balance limitations.

  • Seven-inch LCD touchscreen.
  • Manual mode.
  • Body-part selection.
  • Preset functional programs.

Wi-Fi, Bluetooth, app control, remote operation, and session-history tracking: Not verified for the supplied configuration.

Manufacturer’s WME-01 data

Specification

Supply 100–240

VACFrequency 50/60 Hz

Power consumption 350 W

Confirm the U.S. nameplate rating, grounding, supplied plug, and circuit requirements before electrical preparation. Do not apply electrical instructions from Hue Light’s Sonix or PBM products to this device.

PEMF is an intentional operating technology here; this should not be marketed as a β€œnear-zero EMF” product.

Magnetic field strength, waveform, pulse width, and measurement location are not established in the reviewed specifications. Obtain these details and the manufacturer’s contraindications before making technical comparisons or suitability claims.

The manufacturer lists an audio connection cable among its accessories. This alone does not verify integrated speakers, Bluetooth audio, streaming, or entertainment functions.

Confirm the cable’s purpose before advertising audio capability.

The manufacturer’s reference accessory list includes:

  • Power cord.
  • Rubber leveling pads.
  • Audio connection cable.
  • T-type assembly spanner.
  • Assembly bolts.
  • Printed user manual.

Confirm the complete U.S. packing list, including hardware quantities, before publishing these as guaranteed inclusions.

Plan delivery access and placement around the confirmed equipment dimensions and weight. Obtain instructions covering assembly, leveling, floor suitability, operating clearance, and final safety checks.

Shipping, placement, assembly, and installation services should reflect the approved MERIDIAN estimate.

Model-specific U.S. warranty: Written confirmation required. Hue Light USA’s published warranty schedule names Sonix models VM15 and VC15 but does not separately identify WME-01. Their coverage should not be assumed to apply here.

Certifications: Obtain documentation for the exact supplied model before advertising FDA clearance, medical-device status, or electrical safety certifications.

Follow the current manual for cleaning, inspection, servicing, and approved operating conditions. Request guidance on platform and handrail checks, leveling pads, fasteners, and power-cord inspection.

Before use, review the manufacturer’s restrictions concerning implanted electronic devices, pregnancy, recent procedures, and other medical considerations with an appropriately qualified clinician. This is not an exhaustive contraindication list.

  • FDA Registered
  • CE
  • GMP
  • ISO 9001
  • ISO 13485
  • KC
  • MFDS (Korea)