Saudi Arabia SFDA registration ME0000000537SFDAA00331
Retromax™Plus
Saudi Arabia·MD·Boston Scientific Corporation·Class IIbActiveProduct information
Polymerice Ureteral Stent
Product use
Some of the indications for placement of a Retromax Plus Stent are:
• Extrinsic compression of ureter
• Ureteral incision
• Ureteropelvic junction incision
• Stricture dilatation
Device classification
- Risk Class
- Class IIb
- Product Category
- MD
- Product Type
- MD
Registration information
- Registration ID
- ME0000000537SFDAA00331
- Authorization ID
- GHTF-2019-3183
- Status
- Active
- Expire Date
- February 11, 2024
Manufacturer
- Manufacturer Name
- Boston Scientific Corporation
Model information
- Model ID(s)
- M0061451470 M0061451480 M0061451490 M0061451500 M0061451510
Product accessories
[]
About this record
Access comprehensive regulatory information for Retromax™Plus 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 ME0000000537SFDAA00331 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.
Free DatabasePowered by Pure Global AISFDA Official DataClass IIb