Pure Global

BD ProbeTecโ„ข ET Mycobacterium tuberculosis (ctb) - SFDA Registration ME0000002812SFDAA00076

Access comprehensive regulatory information for BD ProbeTecโ„ข ET Mycobacterium tuberculosis (ctb) 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 ME0000002812SFDAA00076 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.

Free Database
Powered by Pure Global AI
SFDA Official Data
General IVD(Others)
ME0000002812SFDAA00076
BD ProbeTecโ„ข ET Mycobacterium tuberculosis (ctb)
SFDA Registration: ME0000002812SFDAA00076
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Information

For identification of Mycobacterium tuberculosis complex

Product Use

The BD ProbeTecโ„ข ET Mycobacterium tuberculosis Complex (ctb) Culture Identification Reagent Pack, for use with the BD ProbeTec ET System, utilizes Strand Displacement Amplification (SDA) technology for the identification of Mycobacterium tuberculosis complex isolated from culture

Device Classification
Risk Class
General IVD(Others)
Product Category
Chemicals
Product Type
IVD
Registration Information
Registration ID
ME0000002812SFDAA00076
Authorization ID
GHTF-2014-0242
Status
Active
Expire Date
February 24, 2017
Manufacturer
Model Information
Model ID(s)
440621
Product Accessories

[]