European Authorized Representative

European Authorized Representative

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Supplier Details

Med Devices

Free Member  (2009)

[ Ghaziabad, UP, India ]

Supplier has 5 products

Contact Details

Product Description

All Non-European manufacturers of medical equipment who wish to market their products in the EU market under their own name must designate a Regulatory Authorized Representative in order to meet CE requirements.

The European medical device market represents an annual sales volume in excess of 40 Billion Euros . This means, it has become the second largest world-wide, after the United States.

There are, as always, certain obstacles and hurdles to be overcome before the sale of medical devices into Europe. MEDDEVICE can help you to easily gain access to this immense opportunity by assisting you to register for CE-marking and by acting as your Authorized Representative as defined by the European Medical Devices Directives.
MEDDEVICE opens the door to Europe providing you with the best representation possible in the ever-changing environment
of EU legislation

Basic Information

Country:
India
Year Established:
Total Employees:

About Us

MEDDEVICE is committed to provide medical device manufacturers world wide with flexible and well adjusted service packages to assist its clients to comply with EU legislation. The most important aspect of MEDDEVICE is to represent both your company itself and its regulatory affairs interests within the European Union. Our expertise will ensure that you remain in full compliance with EU legislation at all times.
Customer satisfaction is the essential driver in our daily business. We continuously ask our clients what they need from us our clients directly influence our range of services and products on offer. Each client is unique and different MEDDEVICE customizes an individual solution for each one.

We help you to develop and implement cost effective strategies and programs to meet the European requirements for your specific medical device and business objectives. Meddevices maintains a upto date Directory of Medical Devices Manufacturers in the world with clear indication whether the manufacturer has been audited by us or not.

Meddevices has a vision of serving the Medical Device Industry By facilitating
Audits of Medical Devices Manufacturer
European Authorized representative service to foreign establishments
Only Representative service for REACH 2006/1907 (Registration, Evaluation, Authorization and Restriction of Chemicals)
Pre Shipment Inspection
Training Programs
Biocompatibility Testing and Bench Marking
Clinical Research
Software Testing/Verification/Validation

About Us

he most important aspect of MEDDEVICE is to represent both your company itself and its regulatory affairs interests within the European Union. Our expertise will ensure that you remain in full compliance with EU legislation at all times.

Customer satisfaction is the essential driver in our daily business. We continuously ask our clients what they need from us our clients directly influence our range of services and products on offer. Each client is unique and different MEDDEVICE customizes an individual solution for each one.

We help you to develop and implement cost effective strategies and programs to meet the European requirements for your specific medical device and business objectives.

MEDDEVICE to provide medical device manufacturers world wide with flexible and well adjusted service packages to assist its clients to comply with EU legislation.

MEDDEVICE acts as European Authorized Representative for a wide range of companies from start ups to established corporations throughout the world.

Member History

Year Joined:
2009
Membership Type:
Free Member

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