Medtrade receives EU MDR Certification for the Celox CE Range

Omni-stat Medical Inc’s parent company, Medtrade Products Ltd are proud to announce successful receipt of MDR certification for the CELOX CE range of medical devices alongside MDR Quality Management system certification from BSI, a global ISO certification body and the world’s first National Standards Body.

The EU MDR is a medical device regulation that affects all medical devices placed in the European market.
Medtrade has been working vigorously to make sure all existing medical devices’ technical documentation and processes are in accordance with the new regulations.

The team consists of highly skilled experts with a wealth of knowledge in materials science, regulatory, quality requirements and manufacturing processes, and use this to bring to market ground-breaking innovations, that rapidly, safely, and effectively treat life-threatening bleeding in emergency situations.

Russ Mably, Medtrade CEO commented, “We are delighted to receive our MDR certification for the Celox CE range of products. We look forward to continuing to provide our 20 years proven military-grade Celox product range which is designed to stop life-threatening emergency bleeding fast and help save lives.”

About Medtrade:
Medtrade Products Limited, a UK based medical device company established in 1999 with headquarters in Crewe, England provides products and services to the healthcare sector globally.
Medtrade is at the forefront of innovative medical device research and development. With experienced management and scientific leadership within the areas of Hemostasis, Advanced Wound Care and Infection Control, Medtrade designs and delivers pioneering innovative clinically effective products to address unmet clinical needs in pre-hospital and hospital settings.

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Omni-stat Medical Inc

New York – SoHo – Hudson Square,
101 Avenue of the Americas,
8th and 9th Floors,
New York, NY 10013,
USA

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