TXR Tingle X-Ray Systems

All products contained in this web site are manufactured in compliance with the Federal Food, Drug, and Cosmetic Act (the Act), and all applicable or pertinent regulations enforced by the U.S. Food and Drug Administration. Registration, Product Safety and other listing for the devices fall under one or more of the following numbers or categories. FDA Registration Number 1033419, 21 Code of Federal Regulations Subchapter J, ETL Number 54423 ANSI/UL STD 187, UL, CE 0120, CE 0197, CE 0459, ISO 9001-(SGS), ISO 9002, ISO 13485-(SGS), EN46001 (SGS) and EN46002 No 0488.

Substantial Equivalence Letter, 510 (k) Number, Foreign Country Certification Statement, Certificate For Products For Export, and Exporter's Certification Statement can be obtained by request from the TXR Document Section. Specifications can be obtained from our website, product literature, and from the TXR Technical Support Section.

Although the authors of this Web site have made every reasonable effort to be factually accurate, no responsibility is assumed for editorial or clerical errors or error occasioned by honest mistake. All information contained on this Web site is subject to change without prior notice. For comments and concerns, please EMAIL US