Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017674087

FEI Number

3017674087

Entity Name

Quanzhou Enrich Hygienic Products Co., Ltd.

City/State/Country

Quanzhou Fujian, CN

Establishment Address

Building3# A, Economic Development Zone Standard Factory Building, Luojiang District, Quanzhou Fujian 362000, CN

Establishment Type(s)

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

Owner / Operator

Quanzhou Hemei Healthcare Products Co., Ltd. (Owner Number: 10078438)

Owner / Operator Contact Address

Building3# A, Economic Development Zone Standard Factory Building, Luojiang District, Quanzhou, CN-FJ 362000, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Urinal bag with absorbent pad Urinal bag with absorbent pouch Urinal bag Urinal kits Wipes Bedpan liner with absorbent pad Bedpan Liner Toilet bow liner with absorbent pad Super-absorbent pouch drawstring absorbent bags Commode Liner Commode liner with super absorbent pads Toilet bow liner underpad Sanitary Absorbent Napkin Absorbent Core Paper

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FNP	Urinal	General Hospital	Class 1	880.6730	2025-12-21
LRJ	Disinfectant, Medical Devices	General Hospital	Class 1	880.6890	2025-12-21
FOB	Bedpan	General Hospital	Class 1	880.6730	2021-12-29
HHD	Pad, Menstrual, Unscented	Obstetrics/Gynecology	Class 1	884.5435	2021-12-29

Official Correspondent

Yiping Yang

US Agent Details

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

Related Public Records

Same Entity

Quanzhou Hemei Healthcare 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 3017674087. Last updated year: 2026. Please use registration number 3017674087 when referencing this establishment in official correspondence.