CE Certified Massage Bed Cama De Masaje for SPA & Physical Therapy Centers

Name: CE Certified Massage Bed Cama De Masaje for SPA & Physical Therapy Centers
Brand: Wenzhou Pop Relax Co., Ltd.
SKU: 2280037755

Zhejiang, ChinaWenzhou Pop Relax Co., Ltd.

US$950.00

2-29 pieces

US$650.00

30+ pieces

Sample price:US$950.00/unit.Request sample

Product profile

Customization

Available

Fabric

Style

Korean Style

Model NO.

PR-X3

Usage

Health & Beauty, SPA, Medical, SPA Salon Health Center Home

Material

Aluminium

Type

Electric Massage Bed

Folded

Design Style

Contemporary

Feature1

Spine Relax

General Use

Commercial Furniture

Application

SPA,Salon,Health Center,Home

Specific Use

Jade Massage Bed

Model Number

Pr-X3

Function

Infrared Physiotherapy

Voltage

AC110V/AV220V

Temperature Adjustable

30-70℃

Power

370W

Massage Method

Jade Rolling Massage for Spine

Feature2

Upper Body Massage

Transport Package

1 Bed/2 Cartons

Specification

204x75x40cm

Trademark

PopRelax

Origin

China

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: ≤4.27h

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.