• CE, ISO 9001/2008, ISO 13485/2012 standards, with WHO GMP ensuring that 3MC systems, practises, management is tuned to produce high quality products meeting all regulatory standards
  • All 3MC products raw materials have been tested for bio-compatibility, Irritation / Intracutaneous, Sensitization, Cytotoxicity, Acute Systemic Toxicity, Subchronic Toxicity, Genotoxicity, Hemocompatibility, Chronic Toxicity, Implantation and Carcinogenicity. 3MC raw materials are only selected from highly specialized, established sources
  • Clinical trials for all synthetic absorbable sutures to ensure predictable absorption and loss of tensile strength
  • All sutures are beyond compliance to USP metric standards for their physical attributes with international colour coding for sutures
  • Drilled end ribbed needles for better grip in needle holder during surgery
  • Customised suture needle combination
  • Established protocols, standard operating procedures, sterilisation procedures and subsequent stability studies to ensure sutures are made for high quality and they remain so during the entire shelf life
  • 3MC continuously evaluates suture quality and receive feedback from medical professional for improving product standards and providing better outcomes