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ANNULOTOME - SFDA Registration ME0000013693SFDAA00293

Access comprehensive regulatory information for ANNULOTOME 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 ME0000013693SFDAA00293 and manufactured by Richard Wolf 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
ME0000013693SFDAA00293
ANNULOTOME
SFDA Registration: ME0000013693SFDAA00293
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Product Information

ANNULOTOME

Device Classification
Risk Class
1
Product Category
Medical Device
Product Type
1
Registration Information
Registration ID
ME0000013693SFDAA00293
Authorization ID
MDMA-2-2025-0089
Status
Active
Expire Date
January 11, 2028
Manufacturer
Manufacturer Name
Richard Wolf GmbH
Model Information
Model ID(s)
8792.581
Product Accessories

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