Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3031233284

FEI Number

3031233284

Entity Name

ZHEJIANG BOOMINGSHING MEDICAL TECHNOLOGY CO.

City/State/Country

Shaoxing Zhejiang, CN

Establishment Address

26 Kangyang Road, Hangzhou Bay Economic and Technological Development Area, Shangyu District, Shaoxing Zhejiang 312300, CN

Establishment Type(s)

Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Zhejiang Boomingshing Medical Technology Co. (Owner Number: 10090553)

Owner / Operator Contact Address

26 Kangyang Road, Hangzhou Bay Economic and Technological Development Area, Shangyu District, Shaoxing, CN-ZJ 312300, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

inoculation loops and needles

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LXG	Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical Use	Clinical Chemistry	Class 1	862.2050	2024-04-11

Official Correspondent

HuanCahng Li

US Agent Details

Lisa Liu Business: BioMed Resource Email: lisal@bmres.com Phone: (310) 5626975

Related Public Records

Same Entity

Zhejiang Boomingshing Medical Technology Co.

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

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0002-2008	Beckman Coulter Inc	1	FP1000 Cell Preparation System Software versions 1.1 & 1.2, Part Number 624922, for in vitro diagnostic use.
Z-0023-2013	Biomerieux Inc	1	PREVI Isola System, Catalog numbers 29500 and 29500R, bioMerieux, Inc., Durham, NC. Intended to perform the inoculation and streaking of Prepoured Media (PPM) with liquid microbiological samples.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3031233284. Last updated year: 2026. Please use registration number 3031233284 when referencing this establishment in official correspondence.