SHANGHAI YUEYUESHU WOMEN PRODUCTS CO.,LTD.

FDA Device Registration & Listing · Shanghai, CN · Registration 3045009498

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3045009498
FEI Number
3045009498
Entity Name
SHANGHAI YUEYUESHU WOMEN PRODUCTS CO.,LTD.
City/State/Country
Shanghai, CN
Establishment Address
No.1815th Shebei Road, Sheshan Town, Songjiang District, Shanghai 201602, CN
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device
Owner / Operator
Shanghai Yueyueshu Women Products Co.,Ltd. (Owner Number: 10095637)
Owner / Operator Contact Address
No.1815th Shebei Road, Sheshan Town, Songjiang District, Shanghai, CN-NOTA 201602, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Under Pad Sanitary Napkin Adult Diaper Sanitary Napkin Nursing Pad

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FMW Cover, Mattress (Medical Purposes) General Hospital Class 1 880.6190 2026-04-07
HHD Pad, Menstrual, Unscented Obstetrics/Gynecology Class 1 884.5435 2026-04-07
EYQ Garment, Protective, For Incontinence Gastroenterology, Urology Class 1 876.5920 2026-04-07
NRC Pad, Menstrual, Scented, Scented-Deodorized Made Of Common Cellulosic & Synthetic Material W/Established Safety Profile Obstetrics/Gynecology Class 1 884.5425 2026-04-07
NXH Nursing Pad, Cohesive Gel General Hospital Class 1 880.5630 2026-04-07

Official Correspondent

YAN WEI

US Agent Details

Leeyeo Kee Business: Regrek LLC Email: regrek.cs@hotmail.com Phone: (302) 6089028

Related Public Records

Same Entity

Shanghai Yueyueshu Women Products Co.,Ltd.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K823241 Kimberly-Clark Corp. NEW FREEDOM THIN UNSCENTED MAXI PADS 1982-12-28

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3045009498. Last updated year: 2026. Please use registration number 3045009498 when referencing this establishment in official correspondence.
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