Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3034693445

FEI Number

3034693445

Entity Name

HEFEIYONGDASHANGMAOYOUXIANZERENGONGSI

City/State/Country

hefei Anhui, CN

Establishment Address

anhuishenghefeishijingjijishukaifaqufurongshequdanxialuyuqipinglujiaokoucuihuyuan4zhuanglou1danyuan4ceng404, hefei Anhui 230000, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

hefeiyongdashangmaoyouxianzerengongsi (Owner Number: 10092071)

Owner / Operator Contact Address

anhuishenghefeishijingjijishukaifaqufurongshequdanxialuyuqipinglujiaokoucuihuyuan4zhuanglou1danyuan4ceng404, hefei, CN-AH 230000, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Period Swimwear

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NUQ	Pad, Menstrual, Reusable	Obstetrics/Gynecology	Class 1	884.5435	2024-12-02

Official Correspondent

yulian Hu

US Agent Details

mark DU Business: AZUR US Limited Email: markfda@outlook.com Phone: (303) 7319873

Related Public Records

Same Entity

hefeiyongdashangmaoyouxianzerengongsi

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 3034693445. Last updated year: 2026. Please use registration number 3034693445 when referencing this establishment in official correspondence.