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SIMPSON PROBESILVR-PLT MALL D:4/310MM - SFDA Registration ME0000000908SFDAA01890

Access comprehensive regulatory information for SIMPSON PROBESILVR-PLT MALL D:4/310MM in the Saudi Arabia medical device market through Pure Global AI's free database. This Class I device is registered with Saudi Arabia SFDA under registration number ME0000000908SFDAA01890 and manufactured by Aesculap AG.

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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Class I
ME0000000908SFDAA01890
SIMPSON PROBESILVR-PLT MALL D:4/310MM
SFDA Registration: ME0000000908SFDAA01890
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Product Information

surgical probe

Product Use

With the help of uterine probes, the length of the uterus can be determined.

Device Classification
Risk Class
Class I
Product Category
Medical Device
Product Type
MD
Registration Information
Registration ID
ME0000000908SFDAA01890
Authorization ID
MDMA-1-2019-3182
Status
Active
Expire Date
July 09, 2025
Manufacturer
Manufacturer Name
Aesculap AG
Model Information
Model ID(s)
EO020
Product Accessories

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