Saudi Arabia SFDA registration ME0000000975SFDAA00162
Radifocus Guide Wire M
Saudi Arabia·MD·Terumo Europe N.V.·Class IIIActiveProduct information
Guide Wire for angiography
Product use
The Radifocus Guide Wire M is designed to direct a catheter to the desired
anatomical location in the vascular system during diagnostic or interventional
procedures.
Device classification
- Risk Class
- Class III
- Product Category
- MD
- Product Type
- MD
Registration information
- Registration ID
- ME0000000975SFDAA00162
- Authorization ID
- GHTF-2017-1737
- Status
- Active
- Expire Date
- May 26, 2024
Manufacturer
- Manufacturer Name
- Terumo Europe N.V.
Product accessories
[]
About this record
Access comprehensive regulatory information for Radifocus Guide Wire M in the Saudi Arabia medical device market through Pure Global AI's free database. This Class III device is registered with Saudi Arabia SFDA under registration number ME0000000975SFDAA00162 and manufactured by Terumo Europe N.V..
This page provides complete registration details including product category (MD), 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.
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