Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3025376765

FEI Number

3025376765

Entity Name

SHANGHAI QUANFU INTERNATIONAL TRADE CO., LTD.

City/State/Country

Shanghai, CN

Establishment Address

Room 506, 5th Floor, Building 1, No. 4500 Baoqian Road, Jiading Industrial Zone, Shanghai 201821, CN

Establishment Type(s)

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

Owner / Operator

SHANGHAI QUANFU INTERNATIONAL TRADE CO., LTD. (Owner Number: 10086277)

Owner / Operator Contact Address

Room 506, 5th Floor, Building 1, No. 4500 Baoqian Road, Jiading Industrial Zone, Shanghai, CN-SH 201821, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Silicone manual breast pump MOTIF ROAM INSERTS (24/21/19/16MM) MOTIF ROAM TUBING w/CONNECTOR Eye Shield

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HGY	Pump, Breast, Non-Powered	Obstetrics/Gynecology	Class 1	884.5150	2025-01-13
HOY	Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)	Ophthalmic	Class 1	886.4750	2026-04-13

Official Correspondent

Yi Jin

US Agent Details

Creekon Yang Business: SPICA MEDTECH CORP Email: fda.agent@spicagloble.com Phone: (720) 6176666

Related Public Records

Same Entity

SHANGHAI QUANFU INTERNATIONAL TRADE 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 3025376765. Last updated year: 2026. Please use registration number 3025376765 when referencing this establishment in official correspondence.