Regulatory Statements
Pall Medical, part of Cytiva recognizes the importance of supplying information to support our customers in fulfilling regulatory requirements.
Pall Medical ensures that its medical devices are registered in compliance with the requirements established by the local regulatory agencies in in the markets where the products are sold. In addition, Pall Medical actively monitors global regulatory changes to maintain continued compliance with applicable regulatory laws, requirements, and standards throughout the product lifecycle.
Pall Medical assures that purchases of materials conform to specific requirements and that materials are acquired from qualified suppliers. This is achieved through working closely with our suppliers and through a robust qualification process and supplier monitoring process, including continuous supplier audits for materials essential to function.
To view and download statements regarding the environmental compliance of our products, please use the Pall Medical Product Safety Data Information link below.
Pall Medical ensures that its medical devices are registered in compliance with the requirements established by the local regulatory agencies in in the markets where the products are sold. In addition, Pall Medical actively monitors global regulatory changes to maintain continued compliance with applicable regulatory laws, requirements, and standards throughout the product lifecycle.
Pall Medical assures that purchases of materials conform to specific requirements and that materials are acquired from qualified suppliers. This is achieved through working closely with our suppliers and through a robust qualification process and supplier monitoring process, including continuous supplier audits for materials essential to function.
To view and download statements regarding the environmental compliance of our products, please use the Pall Medical Product Safety Data Information link below.