Saudi Arabia SFDA registration ME0000002812SFDAA00071
BD ProbeTec™ ET Samples Tubes and Caps
Product information
Urine Processing Kit
Product use
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
Device classification
- Risk Class
- General IVD(Others)
- Product Category
- Chemicals
- Product Type
- IVD
Registration information
- Registration ID
- ME0000002812SFDAA00071
- Authorization ID
- GHTF-2014-0242
- Status
- Active
- Expire Date
- February 24, 2017
Manufacturer
- Manufacturer Name
- Becton Dickinson and Company
Model information
- Model ID(s)
- 440455
Product accessories
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About this record
Access comprehensive regulatory information for BD ProbeTec™ ET Samples Tubes and 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 ME0000002812SFDAA00071 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.
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