Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003902757

FEI Number

3003902757

Entity Name

JIANGSU SHENLI MEDICAL PRODUCTION CO.,LTD

City/State/Country

CHANGZHOU Jiangsu, CN

Establishment Address

No 20, Changzheng Road, ZHENGLU, CHANGZHOU Jiangsu 213111, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Jiangsu Shenli Medical Production Co., Ltd (Owner Number: 9053084)

Owner / Operator Contact Address

NO 20 CHANGZHENG ROAD, ZHENGLU, CHANGZHOU, CN-JS 213111, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Safety Blood Collection Set CATHETER MEDLINE Y-TYPE TUR/BLADDER IRRIGATION SET

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FMI	Needle, Hypodermic, Single Lumen	General Hospital	Class 2	880.5570	2017-03-17
GBQ	Catheter, Continuous Irrigation	General, Plastic Surgery	Class 1	878.4200	2017-01-19
LJH	System, Irrigation, Urological	Gastroenterology, Urology	Class 2	876.5130	2014-12-16
FHN	Ligator, Hemorrhoidal	Gastroenterology, Urology	Class 2	876.4400	2018-01-08

Official Correspondent

YANG LIQUN

US Agent Details

Charles Mack Business: IRC USA Email: ircfda@gmail.com Phone: (931) 6254938

Related Public Records

Same Entity

Jiangsu Shenli Medical Production 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
K812404	Nu Tech Medical Systems	BUTTERFLY NEEDLE ASSEMBLY	1981-09-09
K000397	Boston Scientific Corp	SPEEDBAND SUPERVIEW MULTIPLE BAND LIGATOR, MODELS 4225, 4228; INJECTION SPEEDBAND SUPERVIEW MULTIPLE BAND LIGATOR, MODEL	2000-03-07

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0002-2022	Bard Peripheral Vascular Inc	2	REF TIN3015, 15G x 79 mm Bone Marrow Aspiration/Intraosseous Infusion Needle, For Single Use Only, Sterile EO, UDI: 10885403043796

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3006850123	JAPAN IRRADIATION SERVICE CO., LTD	Naka-gun Ibaraki, JP
3029328631	PEGASUS IMPORTS	Houston, TX, US
3010621964	ATLAS MEDICAL PRODUCTS LLC	Hialeah, FL, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003902757. Last updated year: 2026. Please use registration number 3003902757 when referencing this establishment in official correspondence.