Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015084765

FEI Number

3015084765

Entity Name

GUANG DONG EDA TECHNOLOGY CO., LTD.

City/State/Country

Dongguan City Guangdong, CN

Establishment Address

No.3, Minolta Road, Shilong Town,, Dongguan City Guangdong 523326, CN

Establishment Type(s)

Manufacture Medical Device,Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Guang Dong EDA Technology Co., Ltd. (Owner Number: 10059483)

Owner / Operator Contact Address

No.3, Minolta Road, Shilong Town, Dongguan City, CN-GD 523326, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

High Flow Nasal Cannula Rescomf Nasal Cannula Purity o3 RESCOMF CPAP Hose Tubing CPAP Tubing RESCOMF Tubing CPAP Hose Tubing

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
CAT	Cannula, Nasal, Oxygen	Anesthesiology	Class 1	868.5340	2022-01-05
LRJ	Disinfectant, Medical Devices	General Hospital	Class 1	880.6890	2019-01-29
BYG	Mask, Oxygen	Anesthesiology	Class 1	868.5580	2020-04-22
BZO	Set, Tubing And Support, Ventilator (W Harness)	Anesthesiology	Class 1	868.5975	2020-04-14

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar corp Email: David.Lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Guang Dong EDA Technology Co., Ltd.

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

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0031-2026	Percussionaire Corporation	1	Phasitron 5, IPV In-Line Valve, (Intrapulmonary Percussive Ventilation) REF: P5-TEE-20 (pack of 20)/ P5-TEE (individual) with In-Line Valve Sentec Instructions for Use

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3015084765. Last updated year: 2026. Please use registration number 3015084765 when referencing this establishment in official correspondence.