Saudi Arabia SFDA registration ME0000001481SFDAA00386
INNOVANCE® PFA-200
Product information
Platelet Aggregation analyser
Product use
The intended use of the INNOVANCE PFA-200 system is to aid in the detection of platelet dysfunction in citrated human whole blood. The system is for in vitro diagnostic use only.
Device classification
- Risk Class
- General IVD(Others)
- Product Category
- Chemicals
- Product Type
- IVD
Registration information
- Registration ID
- ME0000001481SFDAA00386
- Authorization ID
- GHTF-2017-1506
- Status
- Active
- Expire Date
- December 24, 2019
Manufacturer
- Manufacturer Name
- Siemens Healthcare diagnostics products Gmbh
Model information
- Model ID(s)
- B4170-100
Product accessories
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About this record
Access comprehensive regulatory information for INNOVANCE® PFA-200 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 ME0000001481SFDAA00386 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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