LAP GmbH Laser Applikationen achieves MDSAP ISO 13485 certification for excellence in medical device quality management
LAP is pleased to announce its certification under the Medical Device Single Audit Program (MDSAP) to ISO 13485:2016 by TÜV SÜD America.
This internationally recognized standard reaffirms LAP's commitment to quality, safety, and regulatory compliance in the design, development, manufacturing, installation, and servicing of LAP medical products worldwide.
The certification demonstrates LAP’s adherence to stringent quality management practices. MDSAP ensures compliance with regulatory requirements from global markets, including:
- Australia
- Brazil
- Canada
- Japan
- United States
This milestone underscores LAP’s dedication to supporting healthcare providers with innovative products.
“The certification reflects our unwavering commitment to quality and innovation,” says Martin Pfabel, Head of Quality and Regulatory Services. “By adhering to rigorous standards and global regulatory requirements, we continue to ensure that our products and services support the highest standards of care in the medical field. By achieving this certification, we secure optimal conditions for deploying our medical products to important high-tech markets.”
The certification is effective from January 30, 2025, and remains valid through January 29, 2028. Please visit the TÜV SÜD certification database and LAPs Quality and Compliance page for verification and additional details.