What is the elastic recovery rate?

The elastic recovery rate is 97%.

What are the main applications?

It is suitable for denture processing, model making, and oral rehabilitation.

Dental Alginate Impression Material Regular Set High Precision Powder for Dentures

Name: Dental Alginate Impression Material Regular Set High Precision Powder for Dentures
Brand: Foshan Vimel Dental Equipment Co., Ltd.
SKU: 2307845595

Guangdong, ChinaFoshan Vimel Dental Equipment Co., Ltd.

US$2.50

24-239 Bags

US$2.10

240-1,199 Bags

US$2.00

1,200+ Bags

Product profile

Customization

Available

Usage

Denture Processing, Model Making

Usage Times

Disposable

Model NO.

YAXES

Applicable Departments

Oral Rehabilitation Department

Nature

Specialized Instrument Equipment

Certification

Item

Alginate Impression Material

Net Weight

454G

Powder Water Proportion

10g/22ml

Mixing Time

30sec-45sec

Total Working Time

More Than 1min30sec

Time in Mouth

1min30sec

Detail Reproduction Before and After Dis

20μm

Reappearance

50μm

Permanent Deformation

16 %

Compressive Strength

More Than 0.45 MPa

Tear Strength

More Than 0.38n/mm

Transport Package

Standard

Specification

0.5kg

Trademark

VIMEL

Origin

China

Production Capacity

5000pieces/Year

Key features

7 Color Options: Available in 7 optional colors to meet diverse clinical needs.

Fast Working Time: Total working time exceeds 1 minute 30 seconds for efficiency.

3-Year Shelf Life: Long-lasting stability with a guaranteed 3-year shelf life.

CE Certified: Meets CE safety and quality standards for medical devices.

High Compressive Strength: Compressive strength over 0.45 MPa ensures durability.

Easy Mixing: Designed for simple and quick mixing in dental procedures.

Versatile Application: Suitable for denture processing, model making, and orthodontics.

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: ≤5.02hTerms 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.