Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3022815697

FEI Number

3022815697

Entity Name

TIANJIN DEMAX MEDICAL TECHNOLOGY CO., LTD.

City/State/Country

Tianjin, CN

Establishment Address

No.10 Yuanhe Road, Wuqing Development Area, Tianjin 301700, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Tianjin Demax Medical Technology Co., Ltd. (Owner Number: 10085478)

Owner / Operator Contact Address

No.10 Yuanhe Road, Wuqing Development Area, Tianjin, CN-TJ 301700, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

DRD19 DHD0918 DHD0814 DHD1012 DHD0816 Radial Artery Compression Tourniquets DHD1014 DHD0922 DHD0818 DHD1024 DHD0914 DHD0820 DHD1022 DHD0916 DHD0822 DHD0924 DRD17 DHD1016 DHD0920 DHD1020 DHD0812 DHD1018 DRD21 DHD0912 DHRY02 DMK-T-01(ON) DHRY01 DRY03B DMK-T-W3(OFF) DDT02B DHDY03B DPY02 DPY05 DPY04B DPY03B30 DMK-T-W2(OFF) DHDY01B DHDT03B DHRY01B DMK-T-W1(ON) Manifolds DPY01B DDY03B DHRY03B DHDY02B DDY02B DDT03B DRY02B DHRY02B DMK-T-W3(ON) DPY03 DHRY03 Twist Y Connector Kit DDY01B DDT03 DDY02 DMK-T-02(OFF) DHDT01B DHDT01 DPY0230 Namic NaviGuard Push Style Y-Adapter DRY03 DRY02 DPY03B DDT01 DHDT02 DPY02B30 DMK-T-W2(ON) DDY01 DMK-T-W1(OFF) DHDT02B DHDY01 DMK-T-03(ON) DHDY02 DDY03 DDT02 DMK-T-03(OFF) DPY02B DHDY03 DMK-T-01(OFF) Push-Click Y Connector Kit DRY01B DDT01B DMK-T-02(ON) DRY01 DHDT03 DPY01 DPY0330

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DXC	Clamp, Vascular	Cardiovascular	Class 2	870.4450	2023-01-05
DTL	Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass	Cardiovascular	Class 2	870.4290	2022-07-06

Official Correspondent

Xiufang Zhang

US Agent Details

Wen Xu Email: infor@believe-med.com Phone: (443) 8968583

Related Public Records

Same Entity

Tianjin Demax Medical Technology 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
K915301	Advance Medical Designs, Inc.	ADVANCE STOPCOCK/HIGH PRESSURE STOPCOCK	1992-12-11

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3022815697. Last updated year: 2026. Please use registration number 3022815697 when referencing this establishment in official correspondence.