European medical devices Classes

vision In everything we do for the purpose of improving the standard solutions. We believe in air challenges the common procedures and through research and creativity descomplicamos techniques of dental treatments. We do this with products very well designed, innovative and e cient. We ended up revolutionizing the market with excellent performance systems that facilitate the work of thousands of dentists and improve the oral health of people.values


We are part of a European group since 2010 and share our news with the Brazilian market. We guarantee the satisfaction of our customers through technological research, certification of our products and specialized training of our professionals. We are pioneers in the development of Ucla dynamic, original product created in Spain and now available to all surgeons, prosthetists and technicians in the country.


  • Develop and enhance solutions for Implantology sharing our knowledge and our trading systems.
  • Commitment to continuous improvement of our products aiming at the quality of life of patients.
  • Maintain an ethical relationship with our customers and partners while creating value for all shareholders and employees.


Our motivation is the satisfaction of our customers and through continuous improvement of our services shall constitute a worldwide development and distribution solutions, becoming a benchmark for innovation in the dental market.


  • Respect.
  • Honesty.
  • Commitment.
  • Ability to adapt to changes.
  • Experience and teamwork.

All employees of the International Mangran know the values ​​that are part of your corporate culture since its inception. We are convinced that you can only achieve our goals with the daily struggle of our operating team and the dedication of our managers.



CE CERTIFICATE Certifi cation according to the current European legislation for medical devices class I.


0051 Certifi cation according to the current European legislation for medical devices and Class IIA and sterile. Evaluation by the notified stayed.


CERTIFICATE OF FDA Quality Certifi cation obtained by the agency of the U.S. government that validates medical devices.

UNE-EN ISO 13485:2012 Medical devices. Quality Management Systems. Requirements for regulatory fi ns.

UNE-EN ISO 9001:2008 Quality Management Systems. Requirements.

Directory of the European Medical Device & Biomaterials Industry
Book (Elsevier Science Pub Co)
2005-04-04 22:03:48 by -

Not a lap band survivor here, but

It still has a lot of dangers and complications. Here's an online article (5 years old):
FDA panel refuses to endorse obesity 'Lap-Band'
The Lap-Band device
June 19, 2000
Web posted at: 8:45 PM EDT (0045 GMT)
WASHINGTON (CNN) -- A government advisory committee refused to give its seal of approval Monday to a weight-control device that's been used in Europe for seven years - - but has run into medical difficulties during its U.S. trials.
By a 6-4 vote, the Food and Drug Administration advisory committee concluded there was insufficient data to determine whether the device, called Lap-Band, was safe and effective

2003-10-02 06:38:37 by apathetichuman

Sorry for the delay

Had to sleep. Okay, not what you asked for, but, along the same lines. I will find the cream connection and post it later. These articles are all about the companies that pay lots of money for foreskin harvesting. Granted, some of their discoveries are for the betterment of medicine. However, they are all motivated by foreskin for money.
Don't believe it ? Read for yourself - directly from the companies involved - all about the massive foreskin-for-sale industry !
Periscope: Bionic Band-Aid
Newsweek Wednesday, January 13, 1999
Living Human Skin Equivalent Apligraf
Molecule of the Month February 1998
Bioengineered skin wins approval from the FDA
Wound Care newsletter July 1998
The Role of Tissue Engineering in Wound Care
AVF Newsletter American Venous...

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    • # Prepare a Declaration of Conformity. The Declaration of Conformity must contain information adequate for tracing the product back to the manufacturer or the authorized representative in the European Union. It may include a list the directives and standards that your product conforms to, product identification, the manufacturer s name, address and signature. # (If of a type required to be) Register your product in EU Many products, for instance, Class I Medical Devices, are required to be registered in the EU and, if proved, get a Certificate of Registration. Without this Certificate of Registration …