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Martin Medical Packaging

Since its establishment in 2018, Martin Medical Packaging (Zhuhai) Co., Limited has focused on medical sterile packaging. Equipped with a professional technical team and in-house Class 10,000 cleanroom, we manufacture custom medical thermoformed trays, Tyvek lidstock, sterilization pouches and laminated film rolls. Covering R&D, production and sales, we deliver reliable packaging solutions and have earned trust from global medical device customers.
About US
Martin Medical Packaging

Cooperative Enterprise

Since 2018, Martin has partnered with over 800 companies in the medical device and pharmaceutical industries.
Class 10,000 Cleanroom
Class 10,000 Cleanroom
Class 10,000 Cleanroom

Class 10,000 Cleanroom

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WHY CHOOSE US

Cleanroom  Manufacturing
Cleanroom Manufacturing
Our ISO Class 7 clean‑room manufacturing facilities ensure high‑precision thermoformed medical packaging. We deliver consistent, contaminant‑free blister trays lidding materials for sterile medical device packing.
Material & Design Expertise
Material & Design Expertise
We adopt professional medical‑grade mould design and rigorous quality inspection, fully complying with ISO 11607 standards. Each packaging solution guarantees EO/steam sterilization compatibility, safety and stability.
Regulatory & Quality Assurance
Regulatory & Quality Assurance
We hold ISO 13485 certification. All packaging products meet international medical regulatory requirements. Strict document control supports customers’ medical device registration audit.
Customization & OEM Partnership
Customization & OEM Partnership
Focus on custom medical blister tray, vial tray, surgical instrument packaging. Support full‑service from concept design, prototype, mould development to mass‑production for global medical manufacturers.

MARTIN ADVANTAGES

MARTIN ADVANTAGES
Professional Certification

Professional Certification

Our collection of honors highlights our outstanding achievements and continuous pursuit of high standards in our field. We take pride in receiving prestigious certifications
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OUR RECENT NEWS

July 29,2026
Earlier, we mentioned that switching suppliers requires "stability studies." Some readers asked: what is the relationship between accelerated aging and real-time aging? This article will explain it simply.
July 29,2026
These four layers correspond to four questions: How to build the system → What are the requirements → How to select materials → How to conduct testing. Core objective: The establishment and operation of the quality management system must strictly comply with the regulatory requirements of the domestic "Good Manufacturing Practice for Medical Devices".