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GOMCO CIRCUMCISION INSTRUMENT - SFDA Registration ME0000021519SFDAA03208

Access comprehensive regulatory information for GOMCO CIRCUMCISION INSTRUMENT 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 ME0000021519SFDAA03208 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
ME0000021519SFDAA03208
GOMCO CIRCUMCISION INSTRUMENT
SFDA Registration: ME0000021519SFDAA03208
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Product Information

It is a surgical tool used for performing circumcision

Device Classification
Risk Class
1
Product Category
Medical Device
Product Type
1
Registration Information
Registration ID
ME0000021519SFDAA03208
Authorization ID
MDMA-2-2025-0226
Status
Active
Expire Date
January 21, 2028
Manufacturer
Manufacturer Name
Gimmi GmbH
Model Information
Model ID(s)
UC.1494.08,UC.1494.11,UC.1494.13,UC.1494.16,UC.1494.21,UC.1494.26,UC.1494.32
Product Accessories

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