Skip to content

Guangdong Meicen Medical Equipment Co., Ltd.

US Last updated 23 May 2026

Devices
50
Registries
GUDIDEUDAMEDFDA
FDA recalls
0

Catalogue50

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Guangdong Meicen Medical Equipment Co., Ltd. foshan Guangdong · CN FEI 3031218453

What Guangdong Meicen Medical Equipment Co., Ltd. makes

Guangdong Meicen Medical Equipment Co., Ltd. manufactures patient positioning thermoplastic mould materials, thermoplastic arm splint systems, and patient positioning vacuum mattresses. The company also produces central vacuum pumps and patient positioner base plates.

The company's device portfolio includes products categorized as Class I and Class II medical devices. These products are listed in the FDA UDI database, and the company is based in the United States.

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 equipment does Guangdong Meicen Medical Equipment Co., Ltd. manufacture?

The company specializes in patient positioning and support equipment. Their product portfolio includes patient positioning thermoplastic mould materials, thermoplastic arm splint systems, patient positioning vacuum mattresses, central vacuum pumps, and patient positioner base plates.

Where is Guangdong Meicen Medical Equipment Co., Ltd. based?

Guangdong Meicen Medical Equipment Co., Ltd. is based in the United States. This location information is provided as part of the company's official registry data.

How are the devices from Guangdong Meicen Medical Equipment Co., Ltd. classified?

The company's device portfolio consists of both Class I and Class II medical devices. These classifications are determined based on the regulatory requirements for the specific types of equipment they produce.

Which regulatory registries list the devices produced by this manufacturer?

The medical devices manufactured by Guangdong Meicen Medical Equipment Co., Ltd. are listed in the FDA UDI database. This registry is used to track medical devices throughout their distribution and use.

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

Information

Country
US
DUNS number
724689169