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SENTINEL SENTiFIT® – FOB Gold® Latex Wide - HSA Registration DE0509726

Access comprehensive regulatory information for SENTINEL SENTiFIT® – FOB Gold® Latex Wide in the Singapore medical device market through Pure Global AI's free database. This CLASS B IVD medical device is registered under HSA registration number DE0509726 and owned by SENTINEL CH. S.p.A.. The device was registered on September 04, 2024.

This page provides complete registration details including product owner information, registrant details, importer information, and regulatory compliance data from the official Singapore HSA medical device database. Pure Global AI offers free access to Singapore's complete medical device registry, helping global MedTech companies navigate HSA regulations efficiently.

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CLASS B IVD
DE0509726
SENTINEL SENTiFIT® – FOB Gold® Latex Wide
HSA Registration Number: DE0509726
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Product Description

The SENTiFIT® - FOB Gold® latex Wide test allows the quantitative determination of human hemoglobin (Hb) in feces on SENTiFIT 270 Analyzer, and can be used for screening many lower gastrointestinal tract conditions associated with bleeding such as colorectal carcinoma, colon polyps, Crohn’s disease and ulcerative colities. The method is specific for human hemoglobin and no restricted diet (meat-free or peroxidase-free diet) is required.

Device Classification
Device Class
CLASS B IVD
Medical Speciality Area
Gastroenterology & Urology
Registration Information
Registration Number
DE0509726
Registration Date
September 04, 2024
Retention Due Date
September 03, 2025
Product Owner
Short Name
SENTINEL CH. S.p.A.
Address
Via Robert Koch, 2, Milano (MI), 20152, ITALY
Registrant
Address
18 BOON LAY WAY, TRADEHUB 21, #05-105, SINGAPORE 609966
Importer
Address
18 BOON LAY WAY, TRADEHUB 21, #05-105, SINGAPORE 609966
Model Information
Model Name(s)
SENTiFIT® - FOB Gold® latex Wide SENTiFIT® pierceTube FOB Gold® Control Set Wide FOB Gold® Calibrator Wide FOB Gold® Screen Diluent
Model Identifier(s)
1156008 1156188 1157103 1157401 1157501