Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3019793765

FEI Number

3019793765

Entity Name

RESVENT MEDICAL TECHNOLOGY CO., LTD.

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

BC601, Gaoxinqi Factory, District 67 Xingdong Community,Xinan Street, Baoan District, Shenzhen Guangdong 518100, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Resvent Medical Technology Co., Ltd. (Owner Number: 10082384)

Owner / Operator Contact Address

BC601, Gaoxinqi Factory, District 67 Xingdong Community, Xin'an Street Bao'an District, Shenzhen, CN-GD 518100, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

iBreeze PAP (iBreeze 20A; iBreeze 25ST; iBreeze 25STA) Tube

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
QOR	Continuous Ventilator, Minimal Ventilatory Support	Unknown	Class N	N/A	2021-07-19
JAY	Support, Breathing Tube	Anesthesiology	Class 1	868.5280	2022-02-24

Official Correspondent

Harry Wang

US Agent Details

hui hong Business: ABMED MEDICAL TECHNOLOGY INC Email: info@abmed.us Phone: (303) 8000162

Related Public Records

Same Entity

Resvent Medical Technology Co., Ltd.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3019793765. Last updated year: 2026. Please use registration number 3019793765 when referencing this establishment in official correspondence.