What certifications does the product have?

The dental unit is FDA and CE approved.

Can I customize the chair height?

Yes, the height ranges from 440mm to 860mm.

Who handles customs clearance?

Buyers must handle customs clearance or ask their forwarder for help.

Dental Unit Chair FDA Ce Approved PU Leather Computer Control

Name: Dental Unit Chair FDA Ce Approved PU Leather Computer Control
Brand: Foshan Vimel Dental Equipment Co., Ltd.
SKU: 803418465

Guangdong, ChinaFoshan Vimel Dental Equipment Co., Ltd.

US$10.00-850.00

1 Set

Sample price:US$850.00/piece.Request sample

Product profile

Customization

Available

Type

Synthetic Therapy Equipment

Material

PVC

Model NO.

WM-523

Applicable Departments

Oral Rehabilitation Department

Nature

Shared Instrument Equipment

Certification

OEM

Yes

Supply Voltage

110V 60Hz or 220V 50Hz

Water Pressure

0.2MPa-.04MPa

Lowest Position of Dental Chair

440mm

Highest Position of Dental Chair

860mm

Transport Package

Standard Export Carton

Specification

1set/CTN

Trademark

Vimel

Origin

China

HS Code

90184910

Production Capacity

50000sets/Year

Key features

FDA & CE Certified: Complies with international safety standards for dental equipment.

Customizable Voltage: Supports 110V 60Hz or 220V 50Hz for global use.

Durable PU Leather: High-quality synthetic material for long-lasting comfort.

Electric Control System: DC motor with electric valves for precise operation.

Adjustable Chair Position: Range from 440mm to 860mm for patient comfort.

Complete Accessory Set: Includes handpieces, suction, and curing light options.

Manufacturer Direct: Professional R&D and production enterprise in China.

Flexible Payment: Accepts T/T, Western Union, Money Gram, and PayPal.

Company profile

Importers and ExportersExperienced TeamSelf-brandedExhibition Experience

Foshan Vimel Dental Equipment Co., Ltd.

Guangdong, China

Business Type: Manufacturer/Factory, Trading CompanyExport Year: 2015-11-19Average Response Time: ≤5.07hTerms of Payment: T/T, PayPal, Western Union, etc.International Commercial Terms(Incoterms): FOB, CIF, EXW

AI-Powered supplier vetting

SummaryThe supplier produces and sells Class I and Class II medical devices and related products, with one stated production line and in-stock capability. It reports quality assurance, documented corrective and preventive action procedures, written service-assessment procedures, and CE certification capability. The supplier offers extensive customization, ODM, and OEM services, and states that it introduced new products during the past year. After-sales support is backed by an own maintenance centre and after-sale service department, although complaint handling has a procedure but no written records. Manufacturing controls include valid contracts with associated subcontractors and an outsourcing SOP, but there is no ongoing batch quantity reconciliation. Overseas support is limited because no overseas agents, branches, warehouse, or showroom are reported. Financial credibility cannot be determined because only reporting years are provided, without financial results or monetary data.

Supplier typeThe supplier's stated business scope covers production of Class I medical devices, sales of Class I and Class II medical devices, metal structure manufacturing, environmental-protection equipment, hardware wholesale, domestic trade agency, and technology intermediary services. This identifies it as a medical-device manufacturer and distributor with additional industrial activities.

CertificationsThe supplier reports CE capability for sustainable development and product certification and lists another category as “Others” for sustainable development management system certification. CE is explicitly identified, but no specific certification details, certificate numbers, or scope are provided.

After-Sales capabilityThe supplier states that it has an own maintenance centre and after-sale service department, plus a corrective and preventive action procedure with followed records. However, its complaint-handling procedure has no written records, and it reports no overseas agents or branches, overseas warehouse, or overseas showroom, indicating stronger stated domestic/internal support than documented international service coverage.

R&D capabilityThe supplier reports new products during the past year and provides ODM services, demonstrating stated product-development activity. It also reports no available SDK, which limits evidence of software-development or SDK-based integration capability, but does not negate its general R&D capability.

Production capacityProduction capability is supported by the stated medical-device manufacturing scope, in-stock capability, valid contracts with associated subcontractors, an outsourcing SOP, and an average lead time within 15 workdays in both peak and off-season. The supplier reports only one production line and no continuous quantity reconciliation for each batch or volume production, indicating capacity and production-control limitations that should be verified.

Customization capabilityThe supplier explicitly offers customization from samples and designs, full and minor customization, flexible customization, ODM services, and OEM services for popular brands. These statements provide direct evidence of broad customization and contract-manufacturing capability.

Client casesThe supplier states that it provides OEM services for well-known brands and participated in the Beijing Dental Exhibition 2024. No customer names, product-specific case studies, order references, or verifiable performance outcomes are provided, so the breadth and quality of customer experience cannot be fully assessed.