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Salem Sump - SFDA Registration ME0000004584SFDAA00014

Access comprehensive regulatory information for Salem Sump in the Saudi Arabia medical device market through Pure Global AI's free database. This Class IIa device is registered with Saudi Arabia SFDA under registration number ME0000004584SFDAA00014 and manufactured by Covidien LLC.

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
Class IIa
ME0000004584SFDAA00014
Salem Sump
SFDA Registration: ME0000004584SFDAA00014
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Product Information

Dual Lumen Stomach Tube

Product Use

Provide a pathway to aspirate, feed or irritate the stomach.

Device Classification
Risk Class
Class IIa
Product Category
Medical Device
Product Type
MD
Registration Information
Registration ID
ME0000004584SFDAA00014
Authorization ID
MDMA-1-2016-1382
Status
Active
Expire Date
May 26, 2024
Manufacturer
Manufacturer Name
Covidien LLC
Model Information
Model ID(s)
8888264804 8888264820 8888264846 8888264861 8888264887
Product Accessories

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