Smart Thermal Massage Bed for Physiotherapy with Jade Technology Interface

Name: Smart Thermal Massage Bed for Physiotherapy with Jade Technology Interface
Brand: Wenzhou Pop Relax Co., Ltd.
SKU: 2250969735

Zhejiang, ChinaWenzhou Pop Relax Co., Ltd.

US$950.00

2-29 sets

US$650.00

30+ sets

Product profile

Customization

Available

Fabric

Microfiber Leather

Style

European Style

Model NO.

PR-X3

Usage

Health & Beauty, SPA, Foot Massage, Medical

Material

Aluminium Alloy

Type

Whole-length

Folded

Application

Home, Hospital ,SPA ,Hotel

Design Style

Modern

General Use

Commercial Furniture

Specific Use

Massage Table

Place of Origin

Zhejiang,China

Model Number

Pr-X3

Accessory 1

11jade Balls Projector

Accessory2

Health Mat for Foot

Accessory3

EMS Pads

Accessory4

Music Headphone Set

Accessory5

Cloth Cover The Bbed

Accessory6

Side Bag

Transport Package

Carton Box

Specification

125x67x50cm

Trademark

POP RELAX

Origin

China

HS Code

9019101000

Production Capacity

50000

Company profile

Exhibition ExperienceImporters and ExportersYears of Export ExperienceODM Services

Wenzhou Pop Relax Co., Ltd.

Zhejiang, China

CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service Available CertifiedCustomization Options: Customization from Samples, Customization from Designs, etc.Export Year: 2007-10-08 CertifiedNearest Port: Ningbo PortAverage Response Time: ≤3.72h

AI-Powered supplier vetting

SummaryThe supplier is a Class II medical-device and healthcare-products manufacturer with OEM/ODM experience, product customization, and recent new-product development. It reports large monthly production capacity, documented quality, corrective-action, complaint-handling, and finished-product inspection procedures, plus two quality inspectors. CE capability and participation in the CES Fair are reported. However, it has no valid manufacturing-capacity contract with affiliated subcontractors, no inventory, overseas warehouse, overseas showroom, overseas agents or branches, and reports zero countries served through overseas services. Financial information is limited to year labels rather than assessable financial results. Evidence of named customer cases is absent, although OEM service for well-known brands is claimed.

Supplier typeThe supplier describes itself as a manufacturer able to produce large quantities monthly, while its registered scope covers healthcare products, Class II medical devices, and related import/export activities. This supports classification as a healthcare and Class II medical-device manufacturer rather than a purely trading supplier.

CertificationsThe supplier’s business scope includes permitted production of Class II medical devices, and CE is listed under sustainable development and product certification capability. However, no specific certificate number, issuing body, or additional named certification is provided.

After-Sales capabilityDocumented corrective/preventive-action and customer-complaint procedures with records, together with stated technical and after-sales support, indicate an established service process. Coverage is constrained by the absence of overseas agents or branches, overseas warehouses/showrooms, and reported overseas service coverage in zero countries.

R&D capabilityThe supplier reports an R&D department, new products during the past year, OEM/ODM project support, and ODM availability. It also reports no available SDK, so software-development integration capability is specifically limited.

Production capacityThe supplier states that it can produce large quantities monthly and lists performance-testing, sewing, terminal, PAD-printing, and PCB-welding facilities. Finished-product inspection uses written instructions with uniform execution, but there is no valid contract with affiliated subcontractors and no in-stock capability.

Customization capabilityThe supplier explicitly offers flexible, minor, and full customization, including customization from designs and samples. These capabilities are consistently reported in both design-service and facility information.