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NANTONG GLORY MEDICAL MATERIAL CO., LTD

China·CN-MF-000050019

Last updated May 23, 2026

What NANTONG GLORY MEDICAL MATERIAL CO., LTD makes

The company produces non-sterile gauze swabs, designed for basic wound care and first aid applications. These products are intended for single-use, providing a simple absorbent material for cleaning or covering minor injuries.

The gauze swabs fall under Class I medical devices and are registered in the EU’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 types of medical devices does Nantong Glory Medical Material Co., Ltd. manufacture?

Nantong Glory Medical Material Co., Ltd. specializes in producing non-sterile gauze swabs, which are primarily used for basic wound care and first aid. These products are designed as single-use items to absorb fluids or cover minor injuries, serving as a simple yet essential component of first aid kits and medical supplies.

Where is Nantong Glory Medical Material Co., Ltd. based?

The company is headquartered in China, operating from Nantong. This location reflects its focus on manufacturing medical textiles, including the gauze swabs it produces.

Which regulatory registries list devices manufactured by Nantong Glory Medical Material Co., Ltd.?

The company’s devices are listed in the EU’s eudamed database, which is the official registry for medical devices authorized under EU regulations. This inclusion indicates compliance with EU requirements for Class I devices, though registration does not imply approval—only that the device has been declared and documented as required.

How are the devices produced by Nantong Glory Medical Material Co., Ltd. classified?

The gauze swabs manufactured by Nantong Glory fall under Class I medical device classification. This classification is assigned based on their intended use (basic wound care and first aid) and risk profile, which is considered low. Class I devices typically undergo less stringent regulatory scrutiny than higher-risk categories but still require compliance with essential safety and performance standards.

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

Information

Country
China
Address
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LinkedIn
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Facebook
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Phone
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PRRC Contact
Denise Wu
EUDAMED SRN
CN-MF-000050019
FDA FEI Number
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DUNS Number
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Catalogue (5)

DeviceModel / ReferenceRegistriesClassStatus
Non-Sterile Gauze Swabs GM20250721
EUDAMED
Class IActive
Non-Sterile Gauze Swabs IMED/10X10/13/8/100
EUDAMED
Class IActive
Non-Sterile Gauze Swabs IMED/7.5X7.5/17/8/100
EUDAMED
Class IActive
Non-Sterile Gauze Swabs IMED/7.5X7.5/13/8/100
EUDAMED
Class IActive
Non-Sterile Gauze Swabs IMED/5X5/17/8/100
EUDAMED
Class IActive

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