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BEP III System - SFDA Registration ME0000001481SFDAA00384

Access comprehensive regulatory information for BEP III System in the Saudi Arabia medical device market through Pure Global AI's free database. This General IVD(Others) device is registered with Saudi Arabia SFDA under registration number ME0000001481SFDAA00384 and manufactured by Siemens Healthcare diagnostics products Gmbh.

This page provides complete registration details including product category (Chemicals), 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
General IVD(Others)
ME0000001481SFDAA00384
BEP III System
SFDA Registration: ME0000001481SFDAA00384
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Product Information

device for virological and microbiological test

Product Use

for use in blood banks and in virological and microbiological laboratories by trained operators

Device Classification
Risk Class
General IVD(Others)
Product Category
Chemicals
Product Type
IVD
Registration Information
Registration ID
ME0000001481SFDAA00384
Authorization ID
GHTF-2016-2404
Status
Active
Expire Date
December 24, 2019
Model Information
Model ID(s)
OVBI11
Product Accessories

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