01 Components, parts, modules, Original Equipment Manufacturers
07.04 Catheters, cardiac
11 Manufacturing Services
11.16.30 Sterilisation services
13.02 Testing, certification, quality assurance
13.02.02 European "Medical Device Directive" 93/42 conformity assessment services
European "Medical Device Directive" 93/42 conformity assessment services
OSCOR Inc. designs, develops, manufactures and markets a variety of highly specialized implantable cardiac pacing leads, venous access systems and diagnostic catheters.OSCOR Inc. is also leveraging its proprietary lead technologies toward the development of new lead systems for a variety of cardiac and non-cardiac applications.
OSCOR Inc. sells its products in more than 70 countries outside the United States through a combination of direct sales efforts and unaffiliated distributors. Oscor also sells many of its lead and catheter products to leading medical device companies on an Original Equipment Manufacturer (OEM) basis.
QUALITY POLICY Oscor strives to offer products of the highest standards in quality, reliability, service and support. In everything we do we will try to be the most innovative, and the most customer and patient-oriented supplier.
Oscor is committed to continuous quality improvement and will invest in its employees, systems, and technology to provide physicians with the tools necessary to improve patients safety, while reducing recovery times and treatment costs.
Oscor is committed to Employee Empowerment. Management will provide the training, tools and resources necessary to empower employees to make quality decisions. It is the responsibility of each employee to detect and prevent quality issues as well as participate in continuous quality improvement to help meet and exceed customer expectations.
Oscor strives to be an environmentally conscious manufacturer. Our manufacturing focuses on the most efficient and productive use of raw materials and natural resources to minimize any adverse impact on workers and the natural environment.
Oscor is committed to comply with Quality System Requirements and to maintain the effectiveness of the QMS required by ISO 13485 § 5.3, 21 CFR 820 and other applicable regulatory agencies.