RESPIREE PTE LTD

FDA Device Registration & Listing · Singapore Central Singapore, SG · Registration 3020277584

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3020277584
FEI Number
3020277584
Entity Name
RESPIREE PTE LTD
City/State/Country
Singapore Central Singapore, SG
Establishment Address
23 Cantonment Road, Singapore 089743, Singapore Central Singapore 089743, SG
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Respiree PTE LTD (Owner Number: 10087535)
Owner / Operator Contact Address
23 Cantonment Road, singapore 089743, Singapore, SG-NOTA 089743, SG
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

RESPIREE Consumables for RS001.RPM RESPIREE Cardio- respiratory Monitor System Respiree Cardio- respiratory System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BZQ Monitor, Breathing Frequency Anesthesiology Class 2 868.2375 2025-08-14
BZQ Monitor, Breathing Frequency Anesthesiology Class 2 868.2375 2023-03-12

Official Correspondent

Gurpreet Singh

US Agent Details

Cherita James Business: Pro Pharma Group Email: cherita.james@propharmagroup.com Phone: (347) 9540624

Related Public Records

Same Entity

Respiree PTE LTD
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K913749 Edentec Corp. EDENTRACE AIRFLOW 3171/SLEEP LAB AIRFLOW 3170 1992-07-02
K771407 Research Development Corp. LUNG VOLUME & PRESSURE MONITOR 1977-08-04
K122223 Philips Medizin Systeme Boeblingen GmbH NEW: INTELLIVUE CL RESPIRATION POD NEW: SPECIALIZED ASSESSORY: MOBILE CL RESP ATTACHMENT MODIFIED: INTELLIVUE PATIENT MO 2013-04-12

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3020277584. Last updated year: 2026. Please use registration number 3020277584 when referencing this establishment in official correspondence.
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