Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3020969330

FEI Number

3020969330

Entity Name

BEIJING ZHONGYAN TAIHE MEDICAL INSTRUMENT CO., LTD

City/State/Country

Beijing, CN

Establishment Address

4th Floor , Building No.13, No.16 Huankezhong Road, Tongzhou District, Beijing 101102, CN

Establishment Type(s)

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

Owner / Operator

Beijing Zhongyan Taihe Medical Instrument Co., Ltd (Owner Number: 10082737)

Owner / Operator Contact Address

4th Floor , Building No.13 , No.16 Huankezhong Road , Tongzhou District, Beijing, CN-BJ 101102, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ZHONGYAN TAIHE®Acupuncture Needles Acupuncture Needles Press Needles Dry Needles

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MQX	Needle, Acupuncture, Single Use	General Hospital	Class 2	880.5580	2021-10-02

Official Correspondent

Lei Yu

US Agent Details

Ziyu Lu Email: FDA-Agent@h-kun.cn Phone: (347) 8283005

Related Public Records

Same Entity

Beijing Zhongyan Taihe Medical Instrument 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 3020969330. Last updated year: 2026. Please use registration number 3020969330 when referencing this establishment in official correspondence.