Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007125300

FEI Number

3007125300

Entity Name

SHANGHAISUNODEVELOPMENTCOLTD

City/State/Country

Shanghai, CN

Establishment Address

1358 Jiahang Road Jiadlng District, Shanghai 201808, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

DAIO PAPER CORPORATION (Owner Number: 10047337)

Owner / Operator Contact Address

2-60 MISHIMAKAMIYA CHO, SHIKOKUCHUO, JP-38 7990492, JP

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ELIS

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	2015-03-24

Official Correspondent

Ryo Hosoi

US Agent Details

Yusuke Okada Business: Pacific Marketing Alliance, Inc. Email: okada@pmaiusa.com Phone: (310) 6617260

Related Public Records

Same Entity

DAIO PAPER CORPORATION

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3011223701	DAIO PAPER CORPORATION	SHIKOKUCHUO Ehime, JP

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007125300. Last updated year: 2026. Please use registration number 3007125300 when referencing this establishment in official correspondence.