XIAMEN CHUANFUTANG PHARMACEUTICAL CO.,LTD

FDA Device Registration & Listing · xiamen Fujian, CN · Registration 3016765490

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
3016765490
FEI Number
3016765490
Entity Name
XIAMEN CHUANFUTANG PHARMACEUTICAL CO.,LTD
City/State/Country
xiamen Fujian, CN
Establishment Address
2th Factory Buildings,No.3701,xiang an North Road,Xiang anDistrict,xiamen,P.R China, xiamen Fujian 361000, CN
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
XIAMEN CHUANFUTANG PHARMACEUTICAL CO.,LTD (Owner Number: 10083748)
Owner / Operator Contact Address
2th Factory Buildings,No.3701,xiang an North Road,Xiang anDistrict,xiamen,P.R China, xiamen, CN-FJ 361000, CN
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Mask, surgical Respirator, surgical

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FXX Mask, Surgical General, Plastic Surgery Class 2 878.4040 2021-12-15
MSH Respirator, Surgical General, Plastic Surgery Class 2 878.4040 2021-12-16

Official Correspondent

mingta xu

US Agent Details

mark DU Business: AZUR US Limited Email: markFDA@outlook.com Phone: (719) 2013314

Related Public Records

Same Entity

XIAMEN CHUANFUTANG PHARMACEUTICAL 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
K201622 Guangdong Kingfa Sci. & Tech.Co., Ltd. Medical surgical mask 2020-11-24
K881618 3M Company ASEPTEX 1809 FLUID-RESISTANT MOLDED SURGICAL MASK 1988-05-09
K102092 Prestige Ameritech PRO GEAR N95 PARTICULATE FILTER RESPIRATOR & SURGICAL MASK, REGULAR SIZE MODEL RP CERIES 2010-10-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016765490. Last updated year: 2026. Please use registration number 3016765490 when referencing this establishment in official correspondence.
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