About Us

Johari Digital Healthcare Limited is a Corporation, established in 1979, is an international business enterprise with powerful combination of experience and expertise focused to create most advanced medical device solutions. The company has been supplying medical devices to Therapeutic and Medical aesthetic, Life science & Diagnostics markets with its successful venture of Therapeutic & Medical aesthetic product line where thousands of patients were being treated with great results. Our manufacturing facility is ISO 13485:2016, US FDA & GMP (Good Manufacturing Practice) audited. With a state-of-the-art manufacturing facility in an area of 45,000 sq ft, Johari Digital has cutting edge technology developing modern medical devices.

Our Aesthetic treatments comprise of FDA cleared cutting edge bio-electrical stimulation technology and sub dermal therapy, which are backed by internationally tested & clinically proven protocols. In Therapeutic treatments our portfolio is occupied with  a comprehensive assortment of devices like Electrical Stimulator, Portable Electrotherapy Device, Diathermy Machine, Cranial Electrotherapy Stimulator, Joint Stimulator, EMS Stimulator, Combo Stimulator, TENS & CES Stimulator, CPM Machine, Tens Stimulator etc.

Certifications:

• US FDA, ISO 9001:2008, ISO 13485:2003, UL, CE
• US FDA is a pre-market clearance from FDA to assure the safety and effectiveness of the device since they are used over body its utmost important that they perform and safe.
• ISO 9001:2008 is a quality standard for organizations that design, develop, produce or service medical devices. It sets prescribed quality parameters to be maintained for systems.
• ISO 13485:2003 is a single standard for all classes of medical devices. Its scope includes design and manufacturing. It is a key regulatory consideration for allowing medical device manufacturers to market their products around the globe.
• CE mark is a mandatory conformity mark on many products placed on the single market in the European Economic Area. The manufacturer placing the product on the market asserts that the item meets all the essential requirements of the relevant European Directive(s).
• UL is the trusted source across the globe for product compliance. It evaluates products, components, materials and systems for compliance to specific requirements, and permits acceptable products to carry a UL certification mark for US Market.