Pure Global

BFT II Analyzer - SFDA Registration ME0000001481SFDAA00378

Access comprehensive regulatory information for BFT II Analyzer 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 ME0000001481SFDAA00378 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.

Free Database
Powered by Pure Global AI
SFDA Official Data
General IVD(Others)
ME0000001481SFDAA00378
BFT II Analyzer
SFDA Registration: ME0000001481SFDAA00378
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Information

Coagulation analyser

Product Use

The BFT II is a semi-automated device intended for use to determine PT, APTT, TT1, BT1, Fibrinogen, and single factors1. Only for in-vitro diagnostics!

Device Classification
Risk Class
General IVD(Others)
Product Category
Chemicals
Product Type
IVD
Registration Information
Registration ID
ME0000001481SFDAA00378
Authorization ID
GHTF-2017-1506
Status
Active
Expire Date
December 24, 2019
Model Information
Model ID(s)
OVKF03
Product Accessories

[]