SafeGard Medical is established as a key player in the supply of a range of innovative and unique safety medical products to the healthcare industry.
Products are manufactured in accordance with the appropriate standards and where applicable are CE marked in accordance with Medical Devices Directive 93/42/EEC.
Products manufactured by SafeGard are subject to Risk Analysis procedure as described in the standard EN1441:1998 (MDD 93/42/EEC Annex I)
The aim of the risk analysis is to investigate the safety of a medical device by identifying the hazards and estimating the risks associated with the device.
SafeGard Medical has a team of high calibre staff dedicated to promote our products, and deliver pre and post sales training and support.
SafeGard provides a comprehensive and excellent in service program tailored to the specific requirements of the users of SafeGard products.
PRODUCT CERTIFICATIONS AND APPROVAL
SafeGard Medical has been certified and approved by International Organizations.
SECUREGARD RETRACTABLE SYRINGE
EDUCATION AND TRAINING
As an organisation we recognise the importance of providing quality support to the unique products in our portfolio. We offer a range of services:
A Clinical Support Manager will be assigned to the customer to ensure that the users achieve the maximum benefit from the selected products. It will be the responsibility of the Specialist to;
|provide product education for staff on an ongoing basis|
|advise on new product selection|
|introduce new products|
|monitor product effectiveness|
|provide information on product cost effectiveness|
We tailor our in service training to meet your personal needs, facilitated through:
|one to one demonstration|
|personal instruction manuals|