Who We Are

Who We Are

As an independent manufacturer we have 100% control of all our manufacturing processes and as a result we never compromise on quality.

With expertise as a developer, manufacturer and supplier of Microport Devices, we has an exciting product portfolio with the enviable reputation of being able to manufacture and provide the surgeons with all medical devices for specific patients needs.

Our innovative and exciting microport product is updated and expanded in line with technological advances to satisfy the current and future needs of both patients and healthcare professionals.

MicroTek manufactures CE marked medical devices in strict compliance with International manufacturing and regulatory requirements, all products are produced and packaged within state-of-the-art clean room and controlled environments in compliance with EU medical directives and Good Manufacturing Practice(GMP) .

Production facilities have been constructed and maintained in accordance with the WHO GMP requirements for cleanliness. All employees are trained regularly for personal hygiene and clean room environment. Utmost attention is provided to minimize contamination from external sources.

As a part of quality assurance, we carry stringent quality testing at each & every stage of manufacturing processes; intensive In-process quality control for components assembly & packaging helps us in providing Quality products.

Our Vision, Mission and Values Statements

VISION
Within our areas of business we strive to be the preferred partner who sets the standard for the best.
MISSION
We bring the best competences together in order to deliver quality products and services for the benefit of the healthcare sector and patients.
VALUES
Respect, Joy of work, Commitment, Ambitious, Hones

Production Facilities

Our Microport & Instruments are conforming to F.D.A. (Food and Drug Administration) standards and certified according to ISO 13485, ISO 9001, GMP (Good Manufacturing Practice) and all products bear a CE Mark.

Production facilities have been constructed and maintained in accordance with the WHO GMP requirements for cleanliness. Plant operations are maintained for high quality standards by qualified and experienced technical personnel and trained workforce. All employees are trained regularly for personal hygiene and clean room environment. Utmost attention is provided to minimize contamination from external sources.

As a part of quality assurance, we carry stringent quality testing at each & every stage of manufacturing processes; intensive In-process quality control for components assembly & packaging helps us in providing Quality products.

Disposable-Professional-Foreign-Body-Retrieval-Basket-Grasping-Forceps (1)
inspection

Quality Control & Quality Assurance

MicroTek always focuses on quality, quality process starts right from the raw material sourcing & finishes at customer satisfaction. Microtek operates a quality management system compliant with the requirements of ISO 9001:2008 & ISO 13485:2003.

Comprehensive & rigorous quality inspection using physical, chemical, biological & microbiological testing at raw materials stage, during in-process & on finished product helps us in transferring 100% clinically safe products.

Well defined & documented Product Design Dossier & quality assurance procedures, protocols & reports help us in getting fastrack product approval with various regulatory authorities.

Design & Development

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MicroTek always Designs & develops the medical devices so as to fulfill all the requirements of medical device directives. All products are designed & developed according to appropriate & specific criteria’s from various international harmonized standards like Process Standards, System Standards and Product Standard. Selection of biocompatible material is the prime factor considered during product designing

Service Response

service

Modern order processing and product delivery procedures facilitate a rapid response to customer requests and order shipments. This flexibility of approach allows us to manage small orders as efficiently as large bulk shipments. Microtek’s marketing personnel are prompt in responding to customer inquiry & also after sale services and collecting their feedback for continuous improvements

Certifications

In the era of certification, MicroTek has successfully implemented Quality Management System by following and maintaining IS0 9001:2008, ISO 13485:2003, CE Marking as per European Medical Device Directive 93/42/EEC of 14 June 1993 and WHO GMP certification.