NEWS

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1998

Boston

Creation of NATEC Medical LLC in Boston (USA)

Born out of a vision to create value by finding better ways in caring for people with health problems, NATEC Medical LLC was created in Boston, Massachusetts (USA) by a polymer engineer with high entrepreneurial skills.

1999

Innovation

The driving force of this individual rapidly gave astounding results. In a short period of time an innovative product, a balloon for PTCA catheters, was designed, developed and manufactured, ahead of the traditional medical device market at that time. The certification of the product successfully done, it was time to market the product in Europe where it was adopted by a customer and the first orders were placed and delivered.

2000

Port-louis

NATEC Medical set-up & transfer of processing facilities to Mauritius

Yet, manufacturing costs remained expensive.  To remain competitive and to ramp up the production output the strategy was to move to another location with a business-friendly environment for start-ups coupled with a modern infrastructure and a knowledge and skilled based workforce at lower cost.  The decision to relocate the set up to Mauritius.
Strategically positioned, Mauritius is one of the most transparent and financially sound economies in Africa.  It is recognized at a global business centre with an active Export processing zone and an investment friendly tax regime.

2001

2001-thumb

ISO 9001(1994)/13845(1996) certification was rapidly awarded, thanks to our qualified and experienced QA&RA team

2003

2003-thumb

Tamarin© PTCA Catheter is CE Marked

2004

FDA registers the manufacturing facilities under accreditation #3004415014

2006

maurister

Maurister receives its ISO 13485/EN 550 certification for its ETO sterilization process

2006

The sterilization facility gets ISO certified

2006

TB

Tamarin Blue© PTCA catheter is CE Marked

2007

PTCA

Filao© Rx is CE Marked

2008

Filao© OTW is CE Marked

2009

Filao© NC is CE Marked

2010

Maeva

Facilities extension to 2,500m² – 100 employees

The move to Maeva Centre in Ebene, Reduit, is a milestone in the company history. It is a state of the art facilities of 2,500 M2, totaling 700 M2 of clean room of class 1,000 and 10,000.  The facilities are FDA registered and the company follows the GMP, FDA rules 21 CFR part 820.

The R&D department has developed a unique customer focused approach through proactive and professional communication, whilst investing time in the necessary market intelligence and research intelligence of new technologies.  10 % of the company’s turnover is systematically invested in machinery, technology and professional training

2010

CMDCAS

CMDCAS – Canadian Certificate allowing NATEC Medical to sell on the Canadian market

2010

Ebony © 035’’ is CE Marked

2011

Autocad

Crimping service on BMS/DES validated

2011

PTA

Ebony © PTA 0.014” and 0.035” receive 510(k) approval

2011

Crimping BMS/DES is validated

2012

crimping

Crimping service on BVS is validated

2012

510(k) clearance for PTCA Rx

2012

Tamarin© Blue receives 510(k) approval

2013

Coating facility opens.

2013

Health Canada License for PTCA and PTA and ANVISA audited.

2014

In a short time, the company has grown to become a dynamic and reliable business partner, garnering business and earning clients’ trust along the way.  The development of innovative and customer centric product lines and customer satisfaction is the hallmark by which we measure our performance.

We hold ourselves to the highest standard of quality and value.