Our Mission
Mass Syringe Is one of The Largest Factories In Egypt With An Annual Production Capacity Of 400 Million And Is Set To Be The Leader In The Syringe Manufacturing Sector In Egypt, Middle East & Africa.
Mass Syringe Manufacturing Company Ensures That Its Customers Are Provided With The Highest Quality Disposable Syringes, Thereby Helping People Live Healthy Lives.
We Aim To Deliver Superior Growth And Profitability To Our Shareholders By Continuously Improving Productivity And Lowering Costs. Mass Syringe And Its Employees Shall Abide By Applicable Laws And Regulations And Have The Utmost Respect For Mother Nature, For Our Community And For Each Other At All Times.
Vision
We Look forward that Our Products Improve Healthcare Services And Patient Safety. We Will Earn Our Customers’ Trust And Strive To Exceed Their Expectations By Never Compromising From Our Quality And Our Integrity. We Aim To Be An International Leader In The Production Of Disposable Syringes.
Our Story
MASS SYRINGE has established and growing reputation as an innovator and a national leader in many areas of Production of Syringe, The Company was founded in 2015, to manufacture and distribute medical supplies for the Egyptian & foreign Market, The production facility is built in Elzaraby Industrial Zone, Abotige, Assuit, EGYPT (Part No.42) over a 1200 square meters land, owned by the company.
MASS SYRINGE factory is harbouring the following sections:
Quality Policy
MASS for Medical Necessities (MASS SYRINGE) is a leader company in production of sterile Hypodermic Syringes for single use, so its policy is established on the commitment to achieve the legal and customer requirements through the implementation of a quality management system in compliance with international standard EN ISO 13485:2016 and that is reflected from:
Objectives
MASS SYRINGE has developed a Quality Management System to maximize the satisfaction of its customers and to improve the management of the company, MASS SYRINGE Medical Quality Objectives are:
This Manual and the Quality System comply with the International standard EN ISO13485:2016; Quality management systems Requirements for regulatory purposes and MDD 2007/47/EC Medical Device Directive, The purpose of this Manual is to document the Company's Quality policies, to instruct and guide employees whose actions affect product quality, The Manual will inform our customers of the management system that is implemented to assure product quality, The system described in this Manual shall be communicated to all employees in order that they individually understand what is required and how it shall be affected.
The Quality is supported by operating procedures and detailed work instructions to enable customer requirements to be accurately translated.