DITTEL URETHRAL SOUND - SFDA Registration ME0000021519SFDAA03213
Access comprehensive regulatory information for DITTEL URETHRAL SOUND in the Saudi Arabia medical device market through Pure Global AI's free database. This 1 device is registered with Saudi Arabia SFDA under registration number ME0000021519SFDAA03213 and manufactured by Gimmi GmbH.
This page provides complete registration details including product category (Medical Device), 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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SFDA Official Data
1
ME0000021519SFDAA03213
DITTEL URETHRAL SOUND
SFDA Registration: ME0000021519SFDAA03213
Product Information
It is a surgical Instrument used to dilate or explore the urethra
Device Classification
Risk Class
1
Product Category
Medical Device
Product Type
1
Registration Information
Registration ID
ME0000021519SFDAA03213
Authorization ID
MDMA-2-2025-0226
Status
Active
Expire Date
January 21, 2028
Manufacturer
Manufacturer Name
Gimmi GmbHModel Information
Model ID(s)
M.1581.06,M.1581.08,M.1581.10,M.1581.12,M.1581.14,M.1581.16,M.1581.18,M.1581.20,M.1581.22,M.1581.24,M.1581.26,M.1581.28,M.1581.30,M.1581.32,M.1581.34,M.1581.36,M.1581.38,M.1581.40
Product Accessories
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