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Asia Pacific Medical Technology Development Company Limited

US

Last updated May 30, 2026

What Asia Pacific Medical Technology Development Company Limited makes

The company manufactures a centrifugal pump drive unit designed for use in cardiopulmonary bypass systems, including the Anivia SG1000 Pump Console. These devices support extracorporeal circulation during surgical procedures requiring heart-lung bypass.

The company’s centrifugal pump drive units fall under FDA Class II regulation and are listed in the FDA’s Unique Device Identifier (UDI) database. 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 devices does Asia Pacific Medical Technology Development Company Limited manufacture?

The company specializes in centrifugal pump drive units, specifically designed for cardiopulmonary bypass systems. These devices, like the Anivia SG1000 Pump Console, are used to support extracorporeal circulation during surgeries requiring heart-lung bypass.

Where is Asia Pacific Medical Technology Development Company Limited based?

The company is headquartered in the United States. While its name suggests an Asia Pacific focus, its operational base and regulatory filings are tied to the US market.

Which regulatory registries list the company’s devices?

The company’s centrifugal pump drive units, such as the Anivia SG1000 Pump Console, are included in the FDA’s Unique Device Identifier (UDI) database. This registry tracks Class II devices authorized for commercial distribution in the US.

How are the company’s devices classified under FDA regulations?

The company’s centrifugal pump drive units fall under FDA Class II classification. This category applies to devices that pose moderate risk and require special controls beyond general controls to ensure safety and effectiveness.

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

Information

Country
US
Address
—
Website
aniviamed.com
LinkedIn
—
Facebook
—
Phone
7816462900
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
663514869

Catalogue (1)

DeviceModel / ReferenceRegistriesClassStatus
Anivia SG1000 Pump Console SG1000-BBM-001
FDA UDI
Class IIActive

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