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Shenzhen Lifetech Cardio Medical Electronics Co., Ltd.

China·CN-MF-000021613

Last updated May 23, 2026

What Shenzhen Lifetech Cardio Medical Electronics Co., Ltd. makes

Shenzhen Lifetech Cardio Medical Electronics Co., Ltd. manufactures a temporary pacemaker, a short‑term cardiac pacing device intended for use in patients requiring temporary cardiac rhythm support.

The temporary pacemaker is classified as a Class IIb medical device and is listed in the European Union's EUDAMED database. The company 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 does Shenzhen Lifetech Cardio Medical Electronics Co., Ltd. make?

Shenzhen Lifetech Cardio Medical Electronics Co., Ltd. manufactures a temporary pacemaker, which is a short-term cardiac pacing device intended for use in patients requiring temporary cardiac rhythm support. This is the only example device provided in the data, and no other products are mentioned or implied.

Where is Shenzhen Lifetech Cardio Medical Electronics Co., Ltd. based?

The company is based in China, as explicitly stated in the SUMMARY section of the device data. The COUNTRY field also confirms this with the code 'CN', which corresponds to China. No further details about location within China are provided.

Which regulatory registry lists the devices of Shenzhen Lifetech Cardio Medical Electronics Co., Ltd.?

The company's devices are listed in the European Union's EUDAMED database, as stated in both the LISTED IN field and the SUMMARY. EUDAMED is the official system for tracking medical devices in the EU market, and this listing indicates the device has been registered there for regulatory transparency.

How are the devices of Shenzhen Lifetech Cardio Medical Electronics Co., Ltd. classified?

The temporary pacemaker manufactured by the company is classified as a Class IIb medical device, as specified in the DEVICE CLASSES field and reiterated in the SUMMARY. This classification reflects a moderate to high level of risk under the EU medical device regulatory framework, requiring conformity assessment by a notified body.

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

Information

Country
China
Address
1401, Building D1, Nanshan i Park, No.1001, Xueyuan Avenue, Taoyuan Street, Nanshan District, Shenzhen, Guangdong, China
Website
ltcardio.com
LinkedIn
—
Facebook
—
Phone
—
PRRC Contact
Stephy Pan
EUDAMED SRN
CN-MF-000021613
FDA FEI Number
—
DUNS Number
—

Catalogue (1)

DeviceModel / ReferenceRegistriesClassStatus
Temporary Pacemaker 8301
EUDAMEDFDA 510(k)
Class IIbActive

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