Saudi Arabia SFDA registration ME0000014865SFDAA00061
Lumi-Phos PRO
Saudi Arabia·IVD·Beckman Coulter, Inc.·1ActiveProduct information
Buffered solution to be used with Immunoassay systems and reagents
Device classification
- Risk Class
- 1
- Product Category
- IVD
- Product Type
- 2
Registration information
- Registration ID
- ME0000014865SFDAA00061
- Authorization ID
- MDMA-2-2023-0548
- Status
- Active
- Expire Date
- April 13, 2026
Manufacturer
- Manufacturer Name
- Beckman Coulter, Inc.
Model information
- Model ID(s)
- B96000
Product accessories
[]
About this record
Access comprehensive regulatory information for Lumi-Phos PRO in the Saudi Arabia medical device market through Pure Global AI's free database. This 1 device is registered with Saudi Arabia SFDA under registration number ME0000014865SFDAA00061 and manufactured by Beckman Coulter, Inc..
This page provides complete registration details including product category (IVD), 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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