Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015603280

FEI Number

3015603280

Entity Name

NINGBO DECHANG ELECTRICAL APPLIANCE CO.,LTD

City/State/Country

yuyao Zhejiang, CN

Establishment Address

No.2 Heyi Road, Dongjiao Industrial District, Fengshan Street, yuyao Zhejiang 315400, CN

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

Ningbo Dechang Electrical Appliance Co.,Ltd (Owner Number: 10060951)

Owner / Operator Contact Address

Floor 4 Buliding 1, No 21 YongXing East Road, Dongjiao Industrial District, yuyao, CN-ZJ 315400, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KFZ	Humidifier, Non-Direct Patient Interface (Home-Use)	Anesthesiology	Class 1	868.5460	2019-07-18

Official Correspondent

shi huang

US Agent Details

Anna Sun Business: SUN LUNA STAR LLC Email: usa@medpath.pro Phone: (626) 2005096

Related Public Records

Same Entity

Ningbo Dechang Electrical Appliance 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 3015603280. Last updated year: 2026. Please use registration number 3015603280 when referencing this establishment in official correspondence.