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GUYON DILATING BOUGIE - SFDA Registration ME0000021519SFDAA03215

Access comprehensive regulatory information for GUYON DILATING BOUGIE 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 ME0000021519SFDAA03215 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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1
ME0000021519SFDAA03215
GUYON DILATING BOUGIE
SFDA Registration: ME0000021519SFDAA03215
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Product Information

It is a surgical instrument designed for gradual dilation of the urethral tract

Device Classification
Risk Class
1
Product Category
Medical Device
Product Type
1
Registration Information
Registration ID
ME0000021519SFDAA03215
Authorization ID
MDMA-2-2025-0226
Status
Active
Expire Date
January 21, 2028
Manufacturer
Manufacturer Name
Gimmi GmbH
Model Information
Model ID(s)
UV.1604.10,UV.1604.12,UV.1604.14,UV.1604.16,UV.1604.18,UV.1604.20,UV.1604.22,UV.1604.24,UV.1604.26,UV.1604.28,UV.1604.30
Product Accessories

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