MedPlus Group is pleased to announce its role in the development of the new group standard T CAMDI 137-2025, "Medical Non-woven and Medical Composite Materials for Surgery and Medical Devices." The standard has been officially approved and released by the China Medical Device Association, with an effective implementation date of January 8, 2025.

This critical standard was established through a collaborative effort led by key nonwoven manufacturers and clinical leaders from top-tier hospitals. The consortium included MedPlus Group, ProMed, Renji Hospital affiliated with Shanghai Jiao Tong University, and Beijing Tongren Hospital.

T CAMDI 137-2025 sets definitive specifications and quality benchmarks for materials used in surgical and medical device applications. It provides a crucial framework to ensure product consistency, safety, and performance, fostering further innovation and standardization within the medical supply industry.

As a contributing drafter, MedPlus Group underscores its commitment to advancing healthcare quality and strengthening the entire medical supply chain through proactive industry leadership.

T CAMDI 137-2025-《手术和器械防护用医用非织造及复合材料》-发布.pdf

T CAMDI 137-2025-Materiais nãotecidos e compostos para proteção em Cirurgia e Equipamentos Médicos.pdf

T CAMDI 137-2025-Materiales no tejidos y Compuestos para Protección en Cirugía y Equipos Médicos.pdf

T CAMDI 137-2025-Medical Non-woven and Medical Composite Materials for Surgery and Medical Devices.pdf

T CAMDI 137-2025-Non-tissés médicaux et matériaux composites médicaux pour la chirurgie et les dispositifs médicaux.pdf

T CAMDI 137-2025-Медицинские нетканые и композитные материалы для защиты в хирургии и при работе с инструментами.pdf

T CAMDI 137-2025-المواد الطبية غير المنسوجة والمواد المركبة الطبية المستخدمة في الجراحة والأجهزة الطبية.pdf

T CAMDI 137-2025-手術および医療機器防護用の医用不織布及び複合材料.pdf