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Advanced Aseptic Steam Sterilization System for Safe Ampoules
US$5,000.00-20,000.00
1 Piece

Product profile

Customization

Available

After-sales Service

Engineers Available to Service Machinery Overseas, Online Support, video Technical Support

Application

Food Safety, Pharmaceutical Industry

Model NO.

HM AS series

Certification

CE, FDA, GMP, ISO

Condition

New

Customized

Customized

Detection Range

Small Molecules

Material Compatibility

Liquid

Portability

Benchtop

Power Source

Electric Operated

Sensitivity

High Sensitivity

Technology

Ultraviolet-Visible Spectroscopy

User Interface

Touchscreen

Voltage

380V

Transport Package

Seaworthy Packing

Specification

as required

Trademark

HM PHARMACHINE

Origin

Zhejiang China

HS Code

8422303001

Production Capacity

30 Per Year

Key features

Comprehensive Certification: CE, FDA, GMP, and ISO certified for global compliance and safety standards.
24/7 Technical Support: Online support, video technical support, and overseas engineers available.
Customizable Solutions: Customized designs available, including special chamber sizes for dry heat sterilizers.
Advanced Automation: Full automatic control with touchscreen P&ID display and 3-level password access.
Data Integrity Compliance: Meets 21 CFR Part 11 and cGMP standards with computer and recorder data logging.
High Sensitivity Detection: Ultraviolet-Visible Spectroscopy technology for detecting small molecules in liquids.
Versatile Sterilization: Supports steam, dry heat, pulse vacuum, and hot shower sterilization methods.
Global Export Experience: Exporting since 1999 to North America, Europe, Asia, and other global markets.

Company profile

HM Pharmaceutical Engineering & Project (Zhejiang) Co., Ltd.
Importers and ExportersYears of Export Experience
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.

Product Q&A

Q:What certifications does the equipment hold?
A:
The equipment is certified with CE, FDA, GMP, and ISO standards to ensure compliance with international safety and quality regulations.
Q:Is customization available for chamber sizes?
A:
Yes, customization is available. Specifically, for the HM ST-D series Dry Heat Sterilizer, other chamber sizes can be specially designed according to customer requirements.
Q:What after-sales services are provided?
A:
We provide comprehensive after-sales support including online support, video technical support, and engineers available to service machinery overseas.
Q:Does the system comply with data integrity standards?
A:
Yes, the system complies with 21 CFR Part 11 and cGMP standards, featuring computer and recorder data logging for production data.
Q:What are the payment terms?
A:
Terms of payment include LC, T/T, D/P, Western Union, and Money Gram.

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