Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030509408

FEI Number

3030509408

Entity Name

SHENZHEN BOOMINGSHING MEDICAL DEVICE CO. LTD

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

22 Jinxiu East Road, Kengzi Street,Pingshan New District, 103-104,501-502,Building A,Third Sub-park of Rapoo & Space Life Science Park, Shenzhen Guangdong 518118, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Shenzhen Boomingshing Medical Device Co. Ltd (Owner Number: 10089569)

Owner / Operator Contact Address

22 Jinxiu East Road, Kengzi Street,Pingshan New District, 103-104,501-502,Building A,Third Sub-park of Rapoo & Space Life Science Park, Shenzhen, CN-GD 518118, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Labware General

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	2023-12-19

Official Correspondent

Huanchang Li

US Agent Details

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

Related Public Records

Same Entity

Shenzhen Boomingshing Medical Device Co. Ltd

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 3030509408. Last updated year: 2026. Please use registration number 3030509408 when referencing this establishment in official correspondence.