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Flow-Check Pro Fluorospheres - SFDA Registration ME0000000973SFDAA00001

Access comprehensive regulatory information for Flow-Check Pro Fluorospheres 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 ME0000000973SFDAA00001 and manufactured by Beckman Coulter, Inc..

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)
ME0000000973SFDAA00001
Flow-Check Pro Fluorospheres
SFDA Registration: ME0000000973SFDAA00001
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Product Information

Reagent for daily verification of the optical alignment

Product Use

Flow-Check Pro Fluorospheres is a suspension of fluorescent microspheres used for daily verification of the optical alignment and fluidics on the Navios or Cytomics FC 500 Flow Cytometers for Forward Scatter (FS) and FL1- FL4 fluorescence parameters.

Device Classification
Risk Class
General IVD(Others)
Product Category
Chemicals
Product Type
IVD
Registration Information
Registration ID
ME0000000973SFDAA00001
Authorization ID
MDMA-1-2019-0914
Status
Active
Expire Date
December 05, 2024
Manufacturer
Manufacturer Name
Beckman Coulter, Inc.
Model Information
Model ID(s)
A63493
Product Accessories

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