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Restech Resmon PRO FULL - HSA Registration DE0505806

Access comprehensive regulatory information for Restech Resmon PRO FULL in the Singapore medical device market through Pure Global AI's free database. This CLASS B medical device is registered under HSA registration number DE0505806 and owned by Restech Srl. The device was registered on May 20, 2021.

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
DE0505806
Restech Resmon PRO FULL
HSA Registration Number: DE0505806
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Product Description

The Resmon PRO FULL is intended to measure respiratory system impedance using the Forced Oscillation Technique (FOT). Resmon PRO FULL is intended for use with pediatric and adult patients 3 (4 in the US) years of age or older. The device is designed to be used by pulmonologists, general practitioners, nurses, respiratory therapists, laboratory technologists, medical researchers and similarly trained personnel in hospitals, clinics, and private physician offices.

Device Classification
Device Class
CLASS B
Medical Speciality Area
General Hospital
Registration Information
Registration Number
DE0505806
Registration Date
May 20, 2021
Change Notification Approval Date
May 06, 2025
Retention Due Date
May 19, 2025
Product Owner
Short Name
Restech Srl
Address
Via Melchiorre Gioia, 61/63,, 20124 Milano, Italy, ITALY
Registrant
Address
37 UBI CRESCENT, SINGAPORE 408586
Importer
Address
37 UBI CRESCENT, SINGAPORE 408586
Model Information
Model Name(s)
Resmon PRO FULL
Model Identifier(s)
RT1100