DMI
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ABOUT US
Precision in Every Product, Care in Every Life.-
QUALITY FIRST -
ADVANCED MANUFACTURING -
EXPERT TEAM -
BETTER HEALTHCARE TOGETHER
-
10+YEARS
INDUSTRY EXPERIENCE -
20,000+ m²MODERN PRODUCTION
FACILITY -
50+COUNTRIES & REGIONS
SERVED -
100%QUALITY CONTROL
& COMPLIANCE
About DMI
Committed to Clinical Precision & Global Healthcare Improvement
Uncompromising Quality Clinical Precision
Double Medical Instruments Limited is a leading high-tech enterprise specializing in the R&D, production, and sale of disposable medical consumables.
Our facility spans over 15,000 square meters with class 100,000 clean rooms, ensuring every product meets the highest sterile requirements. We take pride in our innovation-driven culture, constantly upgrading our technology to provide healthcare professionals with better tools for patient care.
Company History
Milestones Built on Quality
Worldwide Reach
Serving Healthcare Markets Across the Globe
From Europe to Southeast Asia, the Middle East to Latin America — our products reach distributors in dozens of countries.
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50+
Countries Served
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10+
Years of Export Experience
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500+
Product SKUs
Factory Tour
Inside our precision manufacturing facility
A walkthrough of the clean-room environments, automated assembly, and controlled logistics that power every shipment we send abroad.
Quality Control
Three-stage inspection Zero compromise
Every batch passes through a documented QC framework — from raw material verification to post-sterilization release — because global distributors deserve consistency, not surprises.
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01
Raw Material Inspection
Incoming medical-grade polymers, adhesives, and packaging materials are verified against COA, supplier audit records, and internal physical testing.
- Certificate of Analysis verification
- Biocompatibility pre-screening
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02
In-Process Inspection
Every production shift includes sampled dimensional checks, leak tests, and assembly audits — with real-time deviation logging by QC inspectors.
- AQL sampling at every workstation
- Dimensional & functional testing
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03
Final Release Inspection
Post-sterilization lots are held in quarantine until final QC — including sterility assurance, packaging integrity, and export documentation review.
- EO / Gamma sterilization validation
- Packaging seal & integrity testing
