Communicator™ Surgical Mask with a Clear Window |Case of Ten (10) 40-Mask Dispenser Boxes
This patented, FDA registered device meets ASTM Level 1 surgical mask standards with the added benefit of a fog- resistant clear window for improved communication. Supported by Doctors, Nurses, Dentists, Hygienists, Orthodontists, Interpreters, and other Health Professionals seeking easier communication and exceptional protection.
Designed for use in operating rooms to protect both patient and healthcare workers from the transfer of microorganisms, body fluids, and particulate materials.
- ASTM F2100 Level 1 Protection. >95% bacterial and particle filtration efficiency.
- Comfortable material with elastic earloops and adjustable nosepiece design.
- Not made with latex.
- Easy dispenser box containing 40 single-use, disposable masks.
- Made in the USA for guaranteed highest quality.
- Exclusively from Safe’N’Clear, Inc.
See Facial Expressions. For Medical Practice and General Use.
The Communicator™ is designed to serve as an innovative and affordable protective device for healthcare professionals and consumers who desire clear communication while wearing protective gear.
The product is made in the style of a surgical mask with a clear section in front of the mouth to allow the wearer and those who come in contact a chance to communicate clearly.
Whether you are purchasing the mask for your medical practice or for your family, you can select an order size that fits your needs. Proudly made in the USA with quality as our top priority.
The Communicator™ is manufactured in the USA by the leading domestic manufacturer of surgical masks.
ISO 13485:2003 Certified
ISO 13485:2003 specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer requirements and regulatory requirements applicable to medical devices and related services.
FDA Registered Facility
FDA’s Center for Devices and Radiological Health (CDRH) is responsible for regulating firms who manufacture, repackage, relabel, and/or import medical devices sold in the United States. Our facility underwent FDA inspections to assure compliance with the FDA requirements before it was listed as a registered facility.