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Yancheng Zaichuang Medical Supplies Co.,Ltd

China CN-MF-000037590 Last updated 8 Jun 2026

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Devices
347
Registries
EUDAMED
FDA recalls
0

Catalogue347

Page 1 of 7

Showing 1-50 of 347

Authorised representatives

What Yancheng Zaichuang Medical Supplies Co.,Ltd makes

Yancheng Zaichuang Medical Supplies Co., Ltd manufactures sterile and non-sterile gauze swabs and lap sponges, some of which are designed with X-ray visibility for surgical and medical procedures. These products are intended for wound care, surgical applications, and other clinical uses where absorbency and visibility are required.

The company’s portfolio includes devices classified as Class I and Class IIa under EU regulations, with products listed in 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 Yancheng Zaichuang Medical Supplies Co., Ltd manufacture?

Yancheng Zaichuang Medical Supplies Co., Ltd produces sterile and non-sterile gauze swabs and lap sponges. Some of these products are designed with X-ray visibility, making them suitable for surgical procedures where radiopacity is needed. These devices are primarily used for wound care and absorbency in clinical settings.

Where is Yancheng Zaichuang Medical Supplies Co., Ltd based?

The company is based in China, as indicated in its regulatory and product documentation.

Are any of Yancheng Zaichuang Medical Supplies Co., Ltd’s devices listed in EUDAMED?

Yes, some of Yancheng Zaichuang Medical Supplies Co., Ltd’s devices are listed in the EUDAMED database. This registry includes medical devices that have undergone the necessary regulatory processes for market placement within the European Union, such as classification under EU regulations.

How are Yancheng Zaichuang Medical Supplies Co., Ltd’s devices classified under EU regulations?

Yancheng Zaichuang Medical Supplies Co., Ltd’s devices fall under Class I and Class IIa classifications in the EU regulatory framework. These classifications determine the level of scrutiny and compliance requirements for each device type, with Class I being the lowest risk and Class IIa requiring additional safety assessments.

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

Information

Country
China
Address
1 Fuda Road, Sheyang County, Yancheng City, Jiangsu Province, China
PRRC contact
Hao XU
EUDAMED SRN
CN-MF-000037590