Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008572203

FEI Number

3008572203

Entity Name

MIRACLEAN TECHNOLOGY CO., LTD.

City/State/Country

Shenzhen City Guangdong, CN

Establishment Address

Room 101, Building 1, Angeer Factory, No.4, Hetian Road, Shatian Community, Kengzi street, Pingshan District, Shenzhen City Guangdong 518122, CN

Establishment Type(s)

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

Owner / Operator

Miraclean Technology Co., Ltd. (Owner Number: 10054151)

Owner / Operator Contact Address

Room 101, Building 1, Angeer Factory, No.4, Hetian Road, Shatian Community, Kengzi street, Pingshan District, Shenzhen City, CN-GD 518122, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Absorbent tipped applicator Disposable Cervical Sampling Brush Therapeutic Vaginal Douche Apparatus Disposable Cervical Sampling Brush Absorbent tipped applicator Disposable Sampling Swab Disposable Sampling Swab(Model: 96000G)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KXF	Applicator, Absorbent Tipped, Non-Sterile	General Hospital	Class 1	880.6025	2017-03-20
HED	Douche Apparatus, Vaginal, Therapeutic	Obstetrics/Gynecology	Class 1	884.5900	2017-02-16
KXG	Applicator, Absorbent Tipped, Sterile	General Hospital	Class 1	880.6025	2017-02-16

Official Correspondent

No official correspondent registered.

US Agent Details

Clare Ho Business: SHARE INFO INC. Email: cfrhealthcare@foxmail.com Phone: (929) 4102964

Related Public Records

Same Entity

Miraclean Technology 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 3008572203. Last updated year: 2026. Please use registration number 3008572203 when referencing this establishment in official correspondence.