ISO 13485

This certification specifies requirements for a quality management system for medical device manufacturers. It demonstrates that a company has implemented a quality management system

CE Marking

This marking is a requirement for medical devices sold in the European Union. It indicates that a product meets the safety, health, and environmental protection requirements of the EU.

GMP Certification

This certification demonstrates that a manufacturer follows Good Manufacturing Practices (GMP) to ensure the quality and safety of their products.

The Surgical Instruments Manufacturers Association of Pakistan

The Sialkot Chamber of Commerce & Industry

CNC - Certificate of Complience

ISO 13485:2016

ISO 9001:2015

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