Saudi Arabia SFDA registration ME0000002522SFDAA00173
URETERO-RENO FIBERSCOPE
Saudi Arabia·MD·Olympus Medical Systems Corp.·Class IIaActiveProduct information
ENDOSCOPE
Product use
This instrument has been designed for for endoscopic diagnosis and treatment within the ureter and kidney through a percutaneous route and transurethrally.
Device classification
- Risk Class
- Class IIa
- Product Category
- MD
- Product Type
- MD
Registration information
- Registration ID
- ME0000002522SFDAA00173
- Authorization ID
- MDMA-1-2019-1568
- Status
- Active
- Expire Date
- May 26, 2024
Manufacturer
- Manufacturer Name
- Olympus Medical Systems Corp.
Model information
- Model ID(s)
- URF-P6 / URF-P6R
Product accessories
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About this record
Access comprehensive regulatory information for URETERO-RENO FIBERSCOPE in the Saudi Arabia medical device market through Pure Global AI's free database. This Class IIa device is registered with Saudi Arabia SFDA under registration number ME0000002522SFDAA00173 and manufactured by Olympus Medical Systems Corp..
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 IIa