Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005925370

FEI Number

3005925370

Entity Name

YANGZHONG MEIDI MEDICAL PRODUCTS CO., LTD.

City/State/Country

Yangzhong City Jiangsu, CN

Establishment Address

No. 1088 Hongsheng East Zone, Xinba Science and Tech Park, Yangzhong City Jiangsu 212212, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Yangzhong Meidi Medical Products Co., Ltd. (Owner Number: 10040650)

Owner / Operator Contact Address

No. 1088 Hongsheng East Zone, Xinba Science and Tech Park, Yangzhong City, CN-JS 212212, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HHM	Sound, Uterine	Obstetrics/Gynecology	Class 1	884.4530	2016-08-31
HHK	Curette, Suction, Endometrial (And Accessories)	Obstetrics/Gynecology	Class 2	884.1175	2014-10-26
BYX	Tubing, Pressure And Accessories	Anesthesiology	Class 1	868.5860	2016-08-31

Official Correspondent

Franky Zhang

US Agent Details

Thomas Trimnal Business: Thomas Trimnal Email: thomas@titusmed.com Phone: (803) 3896601

Related Public Records

Same Entity

Yangzhong Meidi Medical Products 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 3005925370. Last updated year: 2026. Please use registration number 3005925370 when referencing this establishment in official correspondence.