KIWA GROUP

93/42/eec, ce marking, conformity assessment, iso 13485, notified body

Company description

We are Kiwa, a world top leader Body specialized in Testing, Inspection and Certification (TIC). With our certification, inspection, testing and training services, we create trust in our customers' products, services, processes, management systems and employees.
Kiwa boasts a wide and in-depth experience from over 20 years in Medical Devices certification, with thousands of products already certified, providing all the necessary services to get complete answers and reliable information on medical devices certification services. Thanks to Kiwa expertise, Medical Companies can demonstrate effective compliance with requirements related to the products, in both mandatory and voluntary certification.

KIWA GROUP

Via Cadriano, 23
40057 Granarolo Dell'emilia (BO)
Italy
Phone: 0039-051-4593419
Fax: 0039-051-763382
info@kiwacermet.it
www.kiwa.com

Contact
Alessia Frabetti
alessia.frabetti@kiwacermet.it
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KIWA GROUP's Products

KIWA GROUP | ISO 13485
Safety and quality are non-negotiable in the medical devices industry – they can literally mean the difference between life and death. With increasingly strict regulatory requirements and expectations from customers and organizations throughout the supply chain, it is critical to demonstrate best practice in quality management processes – and ISO 13485 certification can do that. By partnering with Kiwa, you can use ISO 13485 to ensure the products or services you offer in the medical devices field are in accordance with internationally accepted standards, helping you build trust with customers and meet legal requirements. Contact us to find out more.
KIWA GROUP | TESTING
Our experience makes us leader for medical device certification especially in the following fields:

Diagnosis and Therapy
Surgery
Rehabilitation and Physiotherapy
Odontology
Orthopedics

Contact us to find out more.
KIWA GROUP | CE MARKING
Kiwa, as Notified Body (NBs: 0476, 1984) boasts a wide and in-depth experience as Notified Body from over 20 years in Medical Devices certification. Thanks to Kiwa expertise, Medical Companies can demonstrate effective compliance with requirements related to the products and can access to the European market, as well as obtaining prerequisites to access to other global markets. Moreover, thanks to Kiwa technical expertise, medical devices manufacturers can rely on a trusted partner, able to guarantee the execution of an effective conformity assessment process, which can combine the guarantee of market safeguard with the business tool. Contact us to find out more.

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