Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005128517

FEI Number

3005128517

Entity Name

ZHEJIANG GUANGHUA MEDICAL HOSE TECHNOLOGY CO., LTD.

City/State/Country

Jiaxing City Zhejiang, CN

Establishment Address

No. 31, Kangning Road, Changan Town, Haining City, Jiaxing City Zhejiang 314400, CN

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device

Owner / Operator

ZHEJIANG GUANGHUA MEDICAL HOSE TECHNOLOGY CO., LTD. (Owner Number: 10046476)

Owner / Operator Contact Address

No. 31, Kangning Road, Changan Town, Haining City, Hangzhou Economic Tech Development Zone, Jiaxing City, CN-ZJ 314400, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Medical Hose (GH-2004, GH-2006) CPAP tube (GH-2001) CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY Dental Hose (GH-2008) CPAP tube (GH-2001) Dental Hose (GH-2008) Medical hose (GH-2004,GH- 2006)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BYX	Tubing, Pressure And Accessories	Anesthesiology	Class 1	868.5860	2020-11-05
BZO	Set, Tubing And Support, Ventilator (W Harness)	Anesthesiology	Class 1	868.5975	2021-11-03

Official Correspondent

Li Huang

US Agent Details

Fanny Zhao Business: J & F Technology Service Email: info@jf-yiliao.com Phone: (909) 5100201

Related Public Records

Same Entity

ZHEJIANG GUANGHUA MEDICAL HOSE 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 3005128517. Last updated year: 2026. Please use registration number 3005128517 when referencing this establishment in official correspondence.