What certifications does the equipment have?

The equipment holds CE and RoHS certifications.

What is the maximum pressure for the homogenizer?

The High-pressure Homogenizer supports a maximum working pressure of 1200bar (120Mpa/17400psi).

What are the main markets served?

We export to North America, South America, Eastern Europe, Southeast Asia, Africa, Oceania, Mid East, Eastern Asia, and Western Europe.

Precision Oscillation Mixer for Effective Sample Pre-Processing Equipment

Name: Precision Oscillation Mixer for Effective Sample Pre-Processing Equipment
Brand: HM Pharmaceutical Engineering & Project (Zhejiang) Co., Ltd.
SKU: 2172165075

Zhejiang, ChinaHM Pharmaceutical Engineering & Project (Zhejiang) Co., Ltd.

US$820.00

1 Piece

Product profile

Customization

Available

After-sales Service

Online, at Site

Sample Type

Liquid

Model NO.

HM L-MX-O

Processing Method

Filter

Warranty

1 Year

Environment

Normal Pressure and Temperature

Display

Digital Display

Performance

Automatic

Power Supply

380V

Weight

0-50kg

Certification

CE, RoHS

Customized

Transport Package

Sea Worthy Packing

Specification

as required

Trademark

HM PHARMACHINE

Origin

Zhejiang China

HS Code

9031809090

Production Capacity

30 Per Year

Key features

Customizable Equipment: Product is fully customized to meet specific laboratory requirements.

Wide Application Range: Suitable for medicine, pharmacy, food, cosmetics, and agricultural samples.

High-Pressure Homogenization: Max pressure 1200bar with built-in cooler for efficient sample treatment.

Versatile Mixing Options: Supports manual/automatic mixing with various tube sizes (1.5ml-50ml).

Sterile & Sealed Design: Stainless steel construction with silica gel seals for easy sterilization.

Fast Sample Preparation: Quick digestion and concentration using infrared, microwave, or nitrogen blowing.

Comprehensive Warranty: Provides 1-year warranty with online and on-site after-sales service.

Company profile

Importers and ExportersYears of Export Experience

HM Pharmaceutical Engineering & Project (Zhejiang) Co., Ltd.

Zhejiang, China

Business Type: Manufacturer/FactoryExport Year: 1999-03-18Nearest Port: SHANGHAI,CHINA, NINGBO ,CHINAAverage Response Time: ≤0.72hTerms of Payment: LC, T/T, D/P, etc.International Commercial Terms(Incoterms): FOB, CFR, CIF

AI-Powered supplier vetting

SummaryHM Pharmachine Group presents evidence of established manufacturing, export, and customization capabilities. It operates three production lines, has 6–10 quality-control staff, reports 11–20 years of R&D engineer experience, and has exported for 16 years to broad international markets. Its management-system certifications include ISO9001:2015, ASME, and GMP. Customization is offered from samples, designs, and through full customization, supported by CAD and PORTAL tools and documented R&D inputs, outputs, reviews, verification, and validation. However, important gaps remain: no approved-supplier list, written corrective-action or complaint-handling procedures, valid manufacturing-capacity contracts with related subcontractors, overseas warehouse or showroom capability, environmental-impact assessment report, or available SDK. Financial information is represented only by years rather than performance metrics, so credibility cannot be judged. Customer references are stated, but Fortune 500 collaboration is...

Supplier typeThe supplier is presented as a manufacturing and turnkey project provider for machinery, including ALU cutters, drilling, engraving, lathe, and panel-cutting equipment. It operates three production lines, serves broad international markets, and describes itself as a turnkey solution provider.

CertificationsThe supplier reports ISO9001:2015 certification, with ASME, ISO 9001, and GMP also listed among its management-system certifications. This is explicit evidence of multiple relevant certifications, although the slices do not provide certificate scope or validity details for each item.

After-Sales capabilityThe supplier has in-stock service capacity, overseas agents or branches, and trade-show participation, but it has no written procedures or records for corrective/preventive actions or customer complaint handling. Finished-product inspection instructions exist without written records, indicating a documented-service weakness.

Production capacityThe supplier reports three production lines, in-stock service capability, a broad machinery facility, and 2–3 month lead times in both peak and off-peak seasons. Nevertheless, it lacks a valid contract governing manufacturing capacity with its related subcontractor, which is a stated capacity-management deficiency.

Customization capabilityCustomization is explicitly available from samples, customer designs, and through full customization. The supplier also reports R&D personnel, CAD and PORTAL tools, and documented design-development controls, providing direct support for customization capability.