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Device Registration - Medical Device Bloodborne Pathogen Control

If you are a manufacturer of a needleless system or a sharps device with engineered sharps injury protection and you would like your device to be included on the list, please complete the following registration form and submit with the appropriate registration fee to the Texas Department of State Health Services, P. O. Box 149200, Austin, Texas 78714-9200.

Bloodborne Pathogen Control Program Device Registration (EF23-10857) (PDF, 38KB)


Registration Renewal

The appropriate registration renewal form and renewal fee for each device should be submitted to the department not later than 30 days following the expiration date of the current device registration in order to maintain the device on the department's list of existing needleless systems and sharps devices with engineered sharps injury protection.


Responsibility to Notify the Department of Changes

The device manufacturer shall notify the department in writing of any change that would render the information required in the initial registration application no longer accurate. Upon receipt of a written notification involving a change, the department may update the information contained in its list of needleless systems and sharps devices with engineered sharps injury protection.


Additional Help and Resources

If you have any questions or desire additional information concerning the application process, please contact the Licensing Group at (512) 834-6727

September 2000 Notice to Medical Device Manufacturers (PDF, 28KB)

Last updated May 14, 2020