ViberTEX, Inc. is an authorised distributor of medical protective equipment. Our supplier agreements allow us to sell products globally around the world.

With the rising prices of COVID19, We work with our manufacturers & distributors to ensure that the personal protective equipment is available to our clients, our hospitals, our vendors and distributors.

All equipment is CE & FDA approved & NIOSH Certified.

Keeping Our Employees and Vendors safe is our goal & keeping Our Customers and Our Loved one's safe is our priority with our PPE.

 

 

International - CE marking is a certification mark that indicates conformity with health, safety, and environmental protection standards for products sold within the European Economic Area (EEA). The CE marking is also found on products sold outside the EEA that are manufactured in, or designed to be sold in, the EEA.

USA FDA Registered Certification

FDA Registered Food and Drug Administration, is a government agency responsible for the safety of food, dietary supplements, human drugs, vaccines, blood products and other biologicals, medical devices, radiation-emitting electronics, cosmetics, veterinarian products and tobacco products being sold or manufactured in the United States. The FDA also inspects and enforces regulations related to these industries.

Organizations that manufacture, re-pack or re-label products in the aforementioned industries must register with the FDA, with the exception of cosmetics, where registration is voluntary.

The registration process varies dependent on the industry but generally involves an annual registration in which organizations are required to list all drugs being manufactured, prepared, propagated, compounded, or processed for commercial distribution in the U.S. Inspection results for FDA registered organizations are available on the FDA website.