Saudi Arabia SFDA registration ME0000000537SFDAA00315
Percuflex™
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
- ME0000000537SFDAA00315
- Authorization ID
- GHTF-2019-3183
- Status
- Active
- Expire Date
- February 11, 2024
Manufacturer
- Manufacturer Name
- Boston Scientific Corporation
Model information
- Model ID(s)
- M0061453500 M0061453510 M0061453520 M0061453530 M0061453590 M0061453600 M0061453610 M0061453620 M0061453630 M0061453640 M0061453690 M0061453700 M0061453710 M0061453720 M0061453730 M0061453740 M0061453790 M0061453800 M0061453810 M0061453820 M0061453830 M0061453840 M0061455500 M0061455510 M0061455600 M0061455610 M0061455620 M0061455630 M0061455700 M0061455710 M0061455720 M0061455800 M0061455810
Product accessories
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About this record
Access comprehensive regulatory information for Percuflex™ 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 ME0000000537SFDAA00315 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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