Please browse the following links as a reference for your business.
California Prop 65
Prop 65 requires consumers be informed when they are exposed to certain chemicals. Dynarex adheres to California Prop 65 compliance and labeling.
Unique Device Information (UDI) Labeling
The FDA requires the labeling of most medical devices to include a unique device identifier (UDI). Dynarex is compliant with all FDA labeling standards.
Dynarex follows GS1 standards on class II medical devices to meet FDA requirements for UDI Labeling.
EPA on Medical Waste
For proper disposal and definitions of medical waste, please check with EPA and follow the guidelines outlined.
EPA Home Needle Disposable Guide
For safe needle disposal it is recommended that you reference the EPA for proper guidelines.
OSHA Needlestick/Sharps Injury Facts
Dynarex recommends that any one handling sharp devices reference the U.S. Department OSHA standards with healthcare wide hazards of needlestick/sharps injuries.
US Food and Drug Administration
Visit the FDA to learn about important medical products information.
Latex-Free Labeling Information
Dynarex is compliant with FDA labeling requirements for Latex-Free products.
Packaging Symbol Glossary
Dynarex provides a packaging symbol glossary for your convenience. Please review the link below to access each symbol’s image, title, description, FDA standard and reference number.
Dynarex Corporation has received certification to ISO 13485:2016/MDSAP
The Dynarex Quality Management System complies with FDA 21 CFR Parts 820, 803, 806, and 807 (subparts A to D), Canada Medical Device Regulations – Part 1 -SOR 98/282, and FDA 21 CFR Part 211. Dynarex is committed to continuous improvement, which assures that our customers benefit by receiving products/services that meet their requirements and have consistent product performance.
The Mayo Clinic
The source for medical information and product uses to maintain proper health.
Visit Health Canada to get updates about regulations regarding selling to Canada.