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REFLOTRON GOT (AST) - SFDA Registration ME0000000652SFDAA00017

Access comprehensive regulatory information for REFLOTRON GOT (AST) 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 ME0000000652SFDAA00017 and manufactured by Roche Diagnostics 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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General IVD(Others)
ME0000000652SFDAA00017
REFLOTRON GOT (AST)
SFDA Registration: ME0000000652SFDAA00017
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Product Information

GOT quantitative determination Test

Product Use

Test for the quantitative determination of GOT (AST; ASAT; EC 2.6.1.1) in blood, serum or plasma with Reflotronยฎ.

Device Classification
Risk Class
General IVD(Others)
Product Category
Chemicals
Product Type
IVD
Registration Information
Registration ID
ME0000000652SFDAA00017
Authorization ID
GHTF-2017-0383
Status
Active
Expire Date
May 15, 2023
Manufacturer
Manufacturer Name
Roche Diagnostics GmbH
Model Information
Model ID(s)
10745120202
Product Accessories

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