BD ProbeTec™ ET Caps - SFDA Registration ME0000002812SFDAA00075
Access comprehensive regulatory information for BD ProbeTec™ ET Caps in the Saudi Arabia medical device market through Pure Global AI's free database. This General IVD(Others) device is registered with Saudi Arabia SFDA under registration number ME0000002812SFDAA00075 and manufactured by Becton Dickinson and Company.
This page provides complete registration details including product category (Chemicals), manufacturer information, model details, and regulatory compliance data from the official Saudi Arabia SFDA medical device database. Pure Global AI offers free access to Saudi Arabia's complete medical device registry, helping global MedTech companies navigate SFDA regulations efficiently.
Urine Processing Kit
The BD ProbeTec ET Urine Processing Kit contains urine processing pouches (UPPs) which are designed to remove amplification inhibitors for testing male and female urine specimens with the BD ProbeTec ET Chlamydia trachomatis and Neisseria gonorrhoeae amplified DNA assays on the BD ProbeTec ET System. The UPP may be added at the collection site or laboratory test site
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