What certifications does the product have?

The product is certified with ISO9001, TUV, GMP, ISO, and CE.

Dental Endodontic Endo File Removal System Kit Endo Broken File Removal Instrument

Name: Dental Endodontic Endo File Removal System Kit Endo Broken File Removal Instrument
Brand: Foshan Vimel Dental Equipment Co., Ltd.
SKU: 2079575085

Guangdong, ChinaFoshan Vimel Dental Equipment Co., Ltd.

US$78.00

1-9 Pieces

US$62.00

10+ Pieces

Sample price:US$78.00/piece.Request sample

Product profile

Customization

Available

Condition

New

Certification

ISO9001, TUV, GMP, ISO, CE

Model NO.

VL-ET5

Application

Pet, Adult, Child

Nature

Public Equipment

Feature

Un-waterproof

Usage Times

Non-Disposable

Material

Metal

Transport Package

Box

Trademark

Vimel

Origin

China

Production Capacity

50000

Key features

Multiple Certifications: Product holds ISO9001, TUV, GMP, ISO, and CE certifications for safety and compliance.

Versatile Application: Suitable for use on pets, adults, and children as a public dental equipment tool.

Durable Metal Material: Constructed from high-quality metal, designed for non-disposable, repeated usage.

Fast Delivery: Quick shipping processed within 3-5 working days via express delivery services.

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: ≤4.82hTerms 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.