Saudi Arabia SFDA registration ME0000000975SFDAA00156
Radifocus Guide Wire M Non-vascular
Saudi Arabia·Medical Device·Terumo Europe N.V.·Class IIaActiveProduct information
Non vascular guide wire
Product use
The RADIFOCUS GUIDE WIRE M Non-vascular is intended to assist in the
placement or exchange of devices during non-vascular procedures in
endourology and for the cannulation or insertion of devices into the bile ducts
and pancreatic duct.
Device classification
- Risk Class
- Class IIa
- Product Category
- Medical Device
- Product Type
- MD
Registration information
- Registration ID
- ME0000000975SFDAA00156
- Authorization ID
- GHTF-2016-1510
- Status
- Active
- Expire Date
- December 07, 2020
Manufacturer
- Manufacturer Name
- Terumo Europe N.V.
Product accessories
[]
About this record
Access comprehensive regulatory information for Radifocus Guide Wire M Non-vascular 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 ME0000000975SFDAA00156 and manufactured by Terumo Europe N.V..
This page provides complete registration details including product category (Medical Device), manufacturer information, 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