The Story of Quasar

Quasar specializes in the manufacture of products for the medical device market, catheters, electronics and disposables.
Founded in Hong Kong in 1988 by Boaz Amitai, the company was created to serve as a connection between its European, American and Israeli customers and Chinese electronics manufacturers.
Following four years of acquiring in-depth experience and insight from working with Chinese manufacturers, the growth of its customer base in new fields led to a significant expansion, and a factory was established in Shenzhen, China in 1992. In 2005, Boaz passed the reins to his son Ayal, who now lives with his family in Hong Kong.

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Vision and Values

Quasar Vision

To provide continual, optimal, full turnkey manufacturing solutions through designing trouble-free processes, utilizing our extensive production experience, creative engineering and world class quality.

Quasar Values

To be able to ensure and maintain a high quality of production, we have a solid set of values that guides the way.

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Market Segment

Minimally invasive device

Highly specialized, minimally invasive medical catheters.
Cardio vascular catheters, invasive navigation sensors, disposable colonoscopy catheters.

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Disposable device

Superior quality, single-use medical devices.
Respiratory tube sets, aesthetic tips, aesthetic home use cartridges.

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Electronic device

Complex medical devices that require highly skilled manual, semi and full automated assembly. Blood pressure monitors, Pulse oximeters, Cosmetic home use devices.

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Design for manufacture (DFM) review and pre – process  failure mode  effect  analysis (Pre-PFMEA),which provide a clear process flow diagram (PFD), assembly steps, critical stages  and identify test processes. This preliminary  stage  removes major barriers at  the  initial  mass  production  stage.


Preliminary production portfolio comprising descriptions of the full production process, engineering conclusions, expected challenges and recommendations for production. These advanced processes enable a seamless product transfer from design to production, which ultimately leads to significantly increased efficiency and reduced costs.


Complete manufacturing solutions from the end of the development phase, through the transition from development to production, and on to the mass production phase. Accompanying the product from its inception until it reaches the production line enables not only optimization of the production process and the meeting of schedules and budgets, but also compliance with the high quality standard that Quasar ensures.


The main value that Quasar focuses on throughout the entire production process is quality. Quality manufacturing
in China is a matter that is complex, atypical, and difficult to implement. Quality starts during development and
product planning, but it must be maintained during the transition from the development phase to manufacturing.
Quasar meets the ISO standards relevant to the product, as well as cGMP requirements.

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Learning Center

Medical Device Manufacturing Risk Assessment

Assessing Risk: 5 Tips for Medical Device Risk Management

What is Risk Management Risk assessment in medical device manufacturing is an ongoing responsibility and must be managed and perceived as a top priority in the organization. Risk management is a framework used to identify, evaluate, and mitigate risk or potential failures throughout a medical device’s development life cycle. It is an integral part of the process of medical device development and manufacturing, utilized to ensure a medical devices’ effectiveness, reliability, and safety for patients and operators alike. Risk Management Standards for the Medical Device Industry Risk management standards for the medical device industry, are defined by the ISO 14971 quality standard, as [...]

medical device design and development

Medical Device Product Development: Make the Process Work for Your Product

Medical Device Product Development: How to Make The Process Work For Your Product The medical device design and development process consists of four main phases from start to finish of a medical device’s product lifecycle: conception, design & development, technology transfer, and mass manufacturing. The following is a simple step-by -step approach on how to make the medical device design and development process work for your product, pertaining to every medical device design and development process phase respectively. These factors are key to quick and successful time to market. Conception From as early as the product conception phase, care should be taken to [...]

ISO 13485 Manufacturing

Why ISO 13485 Might Not Be Enough for Your Medical Device Manufacturing Process

ISO 13485 manufacturing is an established quality standard, pertaining to medical device manufacturers. However, as with any quality standard, it is more a set of general guidelines which every manufacturer applies to their own situation according to their status, infrastructure, and working conditions, rather than a recipe for success. There are multiple ways in which it can be applied to each manufacturer’s case, therefore making each medical device manufacturer responsible for guaranteeing their operational effectiveness and success, independent of their ISO 13485 manufacturing certification. An Overview Of ISO 13485 Manufacturing Quality Standard First published in 1996, ISO 13485 in manufacturing is [...]


Hong Kong

19 Cheung Shun St
Cheung Sha Wan, Kowloon

Tel | +852 2803 5262


6 Hayezira St

Tel | +972 4 953 6988

China Shenzhen

Nangang Industrial Park Phase 1
Xili Town, Nanshan District

Tel | +86 755 2765 2055

Ext. 2000|2110

China Dongguan

SSL Medical Park 
Industrial Development Park 

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