C.G. Laboratories, Inc. offers a new Washer Disinfector that is validated to ISO 15883 and fully customizable to any cycle requirement. This washer has the capability to perform critical functions such as cleaning validation, disinfection validation, simulated use (functionality) validation, thermal disinfection validation, and life cycle (continuous-cycle programming capabilities). The FDA has identified specific medical devices that pose a greater likelihood of microbial transmission and a higher risk of infection if not adequately reprocessed, and the washer disinfector serves as a crucial tool to address this concern.

C.G. Laboratories provides comprehensive solutions to fit all reprocessing needs, ensuring that specific product requirements are met. The company’s scientists are equipped to guide and assist in making informed determinations for the reprocessing of medical devices, thereby contributing to a safer healthcare environment.

The washer can be used to evaluate:

  • Cleaning Validation

  • Disinfection Validation
  • Simulated Use (Functionality) Validation

  • Thermal Disinfection Validation
  • Life Cycle (continuous-cycle programming capabilities)

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C.G. Laboratories, Inc.

(817) 270-1945

Why Choose CG Laboratories?

C.G. Labs began in 1983 as a microbiology laboratory founded by Dr. Glenn Crum. In 1996, we relocated to Granbury, TX and expanded our services to include medical device contract manufacturing. We have grown into a multi-service company with three distinct divisions with 19,000 square feet spanning two sites. All our services are current, regulated and quality-driven. We are registered with the FDA and ISO accredited to 13485:2016 and MDSAP.

Our GET MORE objective gives you great customer service, guidance, quality management and access to experts. We strive to exceed your expectations, to meet government regulations and to make the world a safer place. With C.G. Laboratories, you always GET MORE.

C.G. Labs began in 1983 as a microbiology laboratory founded by Dr. Glenn Crum. In 1996, we relocated to Granbury, TX and expanded our services to include medical device contract manufacturing. We have grown into a multi-service company with three distinct divisions with 19,000 square feet spanning two sites. All our services are current, regulated and quality-driven. We are registered with the FDA and ISO accredited to 13485:2016 and MDSAP.

Our GET MORE objective gives you great customer service, guidance, quality management and access to experts. We strive to exceed your expectations, to meet government regulations and to make the world a safer place. With C.G. Laboratories, you always GET MORE.