Saudi Arabia SFDA registration ME0000000537SFDAA00469
Contour™
Saudi Arabia·MD·Boston Scientific Corporation·Class IIbActiveProduct information
Polymeric Ureteral Stent
Product use
The Ureteral Stent is intended to facilitate drainage from the kidney
to the bladder via placement endoscopically or fluoroscopically by a
trained physician.
Device classification
- Risk Class
- Class IIb
- Product Category
- MD
- Product Type
- MD
Registration information
- Registration ID
- ME0000000537SFDAA00469
- Authorization ID
- GHTF-2019-3183
- Status
- Active
- Expire Date
- February 11, 2024
Manufacturer
- Manufacturer Name
- Boston Scientific Corporation
Model information
- Model ID(s)
- M0061802200 M0061802210 M0061802220 M0061802230 M0061802240 M0061802250 M0061802300 M0061802310 M0061802320 M0061802330 M0061802340 M0061802350 M0061802400 M0061802410 M0061802420 M0061802430 M0061802440 M0061802450 M0061805200 M0061805210 M0061805220 M0061805230 M0061805240 M0061805250 M0061805310 M0061805320 M0061805330 M0061805340 M0061805420 M0061805430
Product accessories
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About this record
Access comprehensive regulatory information for Contour™ in the Saudi Arabia medical device market through Pure Global AI's free database. This Class IIb device is registered with Saudi Arabia SFDA under registration number ME0000000537SFDAA00469 and manufactured by Boston Scientific Corporation.
This page provides complete registration details including product category (MD), 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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