GUANGZHOU HAOYIMAI TRADING CO., LTD.

FDA Device Registration & Listing · Guangzhou Guangdong, CN · Registration 3014665853

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
3014665853
FEI Number
3014665853
Entity Name
GUANGZHOU HAOYIMAI TRADING CO., LTD.
City/State/Country
Guangzhou Guangdong, CN
Establishment Address
Room 508, Building 2, No. 383, Huangshi West Road, Baiyun District, Guangzhou, Guangdong, CHINA, Guangzhou Guangdong 510440, CN
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Foreign Private Label Distributor,Export Device to the United States But Perform No Other Operation on Device
Owner / Operator
Guangzhou Haoyimai Trading Co., Ltd. (Owner Number: 10095531)
Owner / Operator Contact Address
Room 508, Building 2, No. 383, Huangshi West Road, Baiyun District, Guangzhou, Guangdong, CHINA, Guangzhou, CN-GD 51440, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Pinknight Water-based lubricant COEROS WATER-BASED LUBRICANT (50ml,100ml,200ml,250ml,300ml)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NUC Lubricant, Personal Obstetrics/Gynecology Class 2 884.5300 2026-03-25

Official Correspondent

Ling Cao

US Agent Details

Dongmei Zhang Business: SOUTH BIOTECH INNOVATION INC Email: jinju321@hotmail.com Phone: (719) 4027027

Related Public Records

Same Entity

Guangzhou Haoyimai Trading Co., Ltd.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K050212 Qualis, Inc. PERSONAL WARMING JELLY 2005-03-17

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014665853. Last updated year: 2026. Please use registration number 3014665853 when referencing this establishment in official correspondence.
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