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Pandemic Response

Our Pandemic Response category offers a comprehensive range of products to support preparedness and response efforts, ensuring healthcare providers, businesses, and governments have access to reliable and compliant supplies. The selection includes disposable and reusable devices essential for patient care, such as thermometers, oximeters, and advanced diagnostic equipment, alongside personal protective equipment (PPE) like masks, gloves, and surgical gowns. Products can be sourced to meet specific regulatory requirements, including standards for the US, EU, and other markets, ensuring compliance and quality. The end-to-end procurement process covers everything from identifying certified manufacturers to coordinating logistics, providing seamless support tailored to specific needs. Long-term supply chain solutions and availability of critical equipment, such as ventilators and sterilization tools, address the unique challenges of pandemic response, enabling effective management of health crises and safeguarding public health with precision and professionalism.

Medical Face Masks Types I, II and IIR

Protective Respirators Types FFP2 & FFP3

Protective Respirators Types FFP2 & FFP3

  • EU Standard EN14683:2019+AC: 2019
  • US Standard ASTM F2100-2019
  • FDA 510(k) or CE (MDR)
  • TÜV or SGS test reports for EU standard products


Protective Respirators Types FFP2 & FFP3

Protective Respirators Types FFP2 & FFP3

Protective Respirators Types FFP2 & FFP3

  • FFP2 & FFP3 NR, NRD
  • EU Standard EN149:2001 + A1:2009
  • US Standard ASTM F302-21
  • KN-Standard GB 2626-2019 KN95
  • FDA 510(k) or CE (MDR)
  • TÜV or SGS test reports for EU standard products

Examination Gloves

Examination Gloves

Examination Gloves

  • ASTM D3577
  • EN455 Standards
  • FDA 510(K)
  • ISO 13485, ISO 9001
  • FDA 510(k) or CE (MDR)
  • TÜV or SGS test reports for EU standard products



Surgical Gowns

Examination Gloves

Examination Gloves

  • CE, FDA, ISO 13485, EN 13795
  • DIN EN ISO 13485:2016, EN 13795:2011+A1:2013, EN ISO 13938-1:1999, EN 29073-3:1992, EN 20811:1992, ISO 9073-10:2003, EN ISO 22610:2006, EN ISO 22612:2005, EN ISO 11737-1:2006, YY/T 0506, ANSI/AAMI PB70
  • FDA 510(k) or CE (MDR)
  • TÜV or SGS test reports for EU standard products



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Tienli Limited

Unit B, 17/F, United Centre, 95 Queensway Admiralty, Hong Kong S.A.R.

Phone: +852 81 99 0926 E-Mail: welcome@tienliglobal.com

Hours (UTC +8hrs)

Mon

09:00 am – 05:00 pm

Tue

09:00 am – 05:00 pm

Wed

09:00 am – 05:00 pm

Thu

09:00 am – 05:00 pm

Fri

09:00 am – 05:00 pm

Sat

By Appointment

Sun

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