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Wuhan BMS Medicaltech Co., Ltd

China·CN-MF-000037241

Last updated May 31, 2026

What Wuhan BMS Medicaltech Co., Ltd makes

Wuhan BMS Medicaltech Co., Ltd manufactures laboratory tubing welders, including automated systems for sealing and joining sterile tubes, as well as metal wire cassettes for medical tubing applications. Their portfolio also includes automatic blood separators designed for laboratory use, which facilitate the separation of blood components in controlled environments.

The company’s devices are classified under Class I and Class II regulations, with products listed in the EU’s eudamed registry and the FDA’s Unique Device Identifier (UDI) database. The manufacturer operates from 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 Wuhan BMS Medicaltech Co., Ltd manufacture?

Wuhan BMS Medicaltech Co., Ltd specializes in laboratory tubing welders, including automated systems for sealing and joining sterile tubes. Their portfolio also includes metal wire cassettes used in medical tubing applications and automatic blood separators designed for laboratory use. These devices are primarily intended for controlled environments where precision and sterility are critical.

Where is Wuhan BMS Medicaltech Co., Ltd based?

The company is based in China, operating from Wuhan. This location influences its regulatory compliance requirements, particularly for devices marketed in international markets like the EU and the US.

Which regulatory registries list devices manufactured by Wuhan BMS Medicaltech Co., Ltd?

Devices from Wuhan BMS Medicaltech Co., Ltd are listed in the EU’s eudamed registry and the FDA’s Unique Device Identifier (UDI) database. These registries help ensure transparency and traceability of medical devices in their respective markets.

How are the devices from Wuhan BMS Medicaltech Co., Ltd classified under medical device regulations?

The company’s devices fall under Class I and Class II classifications. Class I devices generally pose minimal risk and may require fewer regulatory controls, while Class II devices involve moderate risk and typically require additional validation or performance standards to ensure safety and effectiveness.

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

Information

Country
China
Address
818 Gaoxin Avenue, 101, Floor 1, Building B2, Phase II, Block B, Hi-tech Medical Devices Park,818 Gaoxin Avenue, East Lake High-tech Development Zone, Wuhan, China
LinkedIn
—
Facebook
—
Phone
+86-027-65028187
PRRC Contact
Peng Ma
EUDAMED SRN
CN-MF-000037241
FDA FEI Number
—
DUNS Number
545240228

Catalogue (5)

DeviceModel / ReferenceRegistriesClassStatus
Bms Metal Wire Cassette
FDA UDI
Class IIActive
Sterile Tube Welder 0304
EUDAMEDFDA UDI
Class IActive
Metal Wire Cassette 0201
EUDAMED
Class IActive
Automatic Blood Separator 3101
EUDAMED
Class IActive
Automatic Blood Separator 3001
EUDAMED
Class IActive

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