Vision
The DAS vision is to be a world-class and innovative solutions provider to medical device manufacturers. DAS is committed to offering transparent and open relationships so that our customers can easily recognize and evaluate the value-proposition that we create.
Overview
DAS is a contract manufacturer specializing in the design, development, and manufacturing of single-use surgical robotic draping systems, equipment covers, and fluid control pouches. The DAS management team has over 160 years of experience in the development, manufacturing and marketing of sterile equipment covers and draping systems. Our founders are pioneers in the disposable equipment draping market which further enhances our value-add capabilities.
DAS is now a part of UFP Technologies
DAS Medical is now a part of UFP Technologies, an innovative designer and custom manufacturer of components, subassemblies, products, and packaging primarily for the medical market. Utilizing highly specialized foams, films, and plastics, they convert raw materials through laminating, molding, radio frequency welding and fabricating techniques. UFP is diversified by also providing highly engineered solutions to customers in the aerospace, defense, automotive, consumer, electronics, and industrial markets.
You can learn more about the company at www.ufpt.com and www.ufpmedtech.com.
Quality Assurance
DAS Medical will maintain an effective and robust Quality Management System. The goal of our quality system is to ensure we manufacture quality products to the specifications of our customers in compliance with applicable regulations, while focusing on customer service and on-time deliveries. DAS Medical will achieve this through the commitment of management and all associates in the organization.
Regulatory Assurance
FDA
- Owner/Operator registration
- Registered as: manufacturer, contract manufacturer and importer
- 510(k) for surgical equipment covers
ISO
- EN 13485:2003 Certified since October 2012
- Annual surveillance audits completed by our notified body
- All SOP's are in accordance with ISO, CE and Canadian MD requirements
Third Party Audits
- Annual ISO audit
- Customer audits are encouraged
Facilities
Atlanta, Georgia, USA
- 3,000 sq. ft. controlled environmental room (CER) for production and rapid prototyping
- Finished good distribution
- Raw material warehousing and consolidation point for off-shore manufacturing
La Romana, Dominican Republic
- Multiple stand-alone controlled environment rooms (CER) for medical device manufacturing.
- Finished good distribution.
- ARaw material warehousing.