GUANGDONG MAIDI MEDICAL CO.,LTD

FDA Device Registration & Listing · Qingyuan Guangdong, CN · Registration 3014627756

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3014627756
FEI Number
3014627756
Entity Name
GUANGDONG MAIDI MEDICAL CO.,LTD
City/State/Country
Qingyuan Guangdong, CN
Establishment Address
No. 3, Zhihui Road, Guangzhou (Qingyuan) industrial Transfer industrialPark, Shijiao Town, Qingcheng District, Qingyuan Guangdong 511547, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
GUANGDONG MAIDI MEDICAL CO.,LTD (Owner Number: 10057793)
Owner / Operator Contact Address
No. 3, Zhihui Road, Guangzhou (Qingyuan) industrial Transfer industrialPark, Shijiao Town, Qingcheng District, Qingyuan, CN-GD 511547, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K251177
PMA Number
N/A

All Registered Proprietary Names

Packaging Pouch Face Mask Self-Seal Sterilization Pouch and Roll

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
MDM Instrument, Manual, Surgical, General Use General, Plastic Surgery Class 1 878.4800 2018-05-27
QKR Face Mask Within The Scope Of The Face Mask And Barrier Face Covering Enforcement Policy Or Face Mask Umbrella Eua Unknown Class N N/A 2020-03-31
JOJ Indicator, Physical/Chemical Sterilization Process General Hospital Class 2 880.2800 2025-12-18
FRG Wrap, Sterilization General Hospital Class 2 880.6850 2025-12-18

Official Correspondent

Mingdong Chen

US Agent Details

Leeyeo Kee Business: Regrek LLC Email: regrek.cs@hotmail.com Phone: (302) 6089028

Related Public Records

Same Entity

GUANGDONG MAIDI MEDICAL 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-0027-2007 N/A 2
3M Comply 1248 Gas Plasma Chemical Indicator Strips for use in STERRAD 100, STERRAD 100S and STERRAD 50 Sterilization Systems. Indicator for hydrogen peroxide sterilant.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014627756. Last updated year: 2026. Please use registration number 3014627756 when referencing this establishment in official correspondence.
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