Import Anti-Fog Surgical Face Mask Level 3 & Type Iir — Buy in Bulk from Supplier in Taiwan

The Anti-Fog Surgical Face Mask Level 3 & Type IIR from Motex Healthcare Corp. is a medical-grade respiratory protection device designed to prevent fogging on glasses and surgical instruments. It achieves a bacterial filtration efficiency (BFE) greater than 98%, providing a high level of protection against airborne bacteria and viruses. The Type IIR rating ensures resistance to fluid penetration, making it suitable for surgical and high-risk medical environments.

The mask incorporates a multi-layer structure, typically including a meltblown filtration layer sandwiched between non-woven outer layers. The anti-fog feature is achieved through a hydrophilic coating or additive that reduces surface tension, preventing condensation buildup. Standard industry specifications for such masks include a breathability (delta P) of less than 60 Pa/cm² and a fluid resistance of at least 120 mmHg, as per EN 14683 norms.

Primary users include healthcare professionals in surgical, dental, and emergency medical settings. The mask is also used in laboratories and other environments where fluid resistance and high filtration are required. Trade terms for Taiwanese suppliers often include FOB Keelung or Taichung, with bulk orders packed in cartons. Buyers should confirm the exact packaging configuration and lead times, as these can vary based on order volume.

Motex Healthcare Corp. is a Taiwan-based supplier specializing in medical protective gear, including surgical masks and other personal protective equipment. The company operates within the imported-tier category, indicating experience in international trade. Its harbor trust tier suggests reliability in fulfilling export orders, though specific details such as production capacity or certifications are not provided in the profile.

The supplier’s address is not listed in the available data, but its origin in Taiwan positions it well for serving global markets, particularly in Asia and North America. Buyers should request additional information such as ISO 13485 certification, FDA 510(k) clearance, or CE marking to confirm compliance with medical device regulations. The absence of response rate data does not necessarily indicate poor service, but direct communication is recommended for verification.