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FOSHAN ANCHENG MEDICAL EQUIPMENT TECHNOLOGY CO., LTD

China·CN-MF-000041913

Last updated May 23, 2026

What FOSHAN ANCHENG MEDICAL EQUIPMENT TECHNOLOGY CO., LTD makes

Foshan Ancheng Medical Equipment Technology Co., Ltd. manufactures mobility aids and assistive devices, including shower chairs, commode chairs, walkers, rollators, canes and crutches, manual wheelchairs, and electric power wheelchairs. These products are designed to support independent movement and daily living for users with limited mobility or disabilities.

The company’s products are classified as Class I medical devices and are registered in the EU through the euDAMED database. The manufacturer is based in China.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does Foshan Ancheng Medical Equipment Technology Co., Ltd. manufacture?

Foshan Ancheng Medical Equipment Technology Co., Ltd. specializes in mobility aids and assistive devices. Their product range includes shower chairs, commode chairs, walkers, rollators, canes and crutches, manual wheelchairs, and electric power wheelchairs. These devices are designed to help users with limited mobility or disabilities maintain independence in daily activities.

Where is Foshan Ancheng Medical Equipment Technology Co., Ltd. based?

The company is headquartered in China, as indicated in their regulatory information. This location is relevant for understanding the origin of their products and potential regulatory pathways they may follow.

How are the devices manufactured by Foshan Ancheng classified under medical device regulations?

The devices produced by Foshan Ancheng Medical Equipment Technology Co., Ltd. are classified as Class I medical devices. This classification is typically assigned to low-risk products, such as mobility aids, which generally pose minimal risk to users when used as intended. Classification determines regulatory requirements, and Class I devices often undergo less stringent scrutiny than higher-risk categories.

Are the company’s devices listed in any regulatory registries, and if so, which ones?

Yes, the company’s devices are registered in the euDAMED database, which is the European Union’s medical device registry. This listing indicates that their products have been formally declared or certified for placement on the EU market, though it does not imply approval—only that they meet the necessary regulatory requirements for that market.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
China
Address
No.3, Ground Floor,Workshop 11,No. 5, Hongtu Road, Songxia Industrial Park, Songgang, Shishan Town, Nanhai District,, Foshan City ,Guangdong Province, China
Website
qq.com
LinkedIn
—
Facebook
—
Phone
—
PRRC Contact
meihua Yang
EUDAMED SRN
CN-MF-000041913
FDA FEI Number
—
DUNS Number
—

Catalogue (10)

DeviceModel / ReferenceRegistriesClassStatus
Shower Chair AC782L
EUDAMED
Class IActive
Commode Chair AC691
EUDAMED
Class IActive
Walker AC912L-5
EUDAMED
Class IActive
Electric wheelchair WB-10001
EUDAMED
Class IActive
Rollator AC802L
EUDAMED
Class IActive
Stick & Crutch AC911L
EUDAMED
Class IActive
Manual Wheelchair AC-A06
EUDAMED
Class IActive
Electric Power Wheelchair AC-D01L
EUDAMED
Class IActive
Commode chair WB-2001
EUDAMED
Class IActive
Rollator WB-2407
EUDAMED
Class IActive

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