At JE Petersen, we pride ourselves on quality. We believe that a culture of excellence is the most important component of a medical device manufacturer. We strive daily to provide the highest quality products and services to our customers.
THE OBJECTIVE OF JE PETERSEN IS TO PROVIDE QUALITY PRODUCTS AND SERVICES THAT MEET THE NEEDS AND EXPECTATIONS OF OUR CUSTOMERS, PARTNERS, AND REGULATORY BODIES. WE OPERATE IN AN ENVIRONMENTALLY RESPONSIBLE AND SUSTAINABLE MANNER. WE ARE COMMITTED TO MEETING ALL APPLICABLE REQUIREMENTS AND CONTINUALLY IMPROVING THE EFFECTIVENESS OF THE QUALITY MANAGEMENT SYSTEM.
JE Petersen is an FDA registered manufacturer, fully compliant with all FDA 21 CFR 820 requirements.
ISO 13485:2012 Certified
From our certification: JE Petersen has been assessed and deemed to comply with the provisions of [ISO 13485:2012] in respect of scope of operations given below:
The manufacturing, distribution and servicing of active medical systems for neurological diagnostics, active and non-active surgical instruments and suction catheters for plastic, orthopedic, thoracic and general surgery.
Download our Certificate: ISO 13485:2012
IEC 60601 3rd Edition Compliant
JE Petersen is fully compliant with IEC 60601-1 3rd Edition including RoHS compliance. JE Petersen is committed to producing high-quality products in a safe and environmentally sustainable manner.