Woundexpress

FDA UDI

Class II (US FDA UDI)

by Huntleigh Healthcare , Ltd.

Identity

Trade Name: WOUNDEXPRESS FDA UDI
Generic Name: Sequential venous compression system FDA UDI
Device Name: WOUNDEXPRESS IPC PUMP USA FDA UDI
Model / Reference: WE100P-USA FDA UDI
Description: WOUNDEXPRESS IPC PUMP USA FDA UDI

Identifiers

Catalog Number: WE100P-USA FDA UDI
Primary DI / UDI-DI: 05051968042941 FDA UDI
FDA Product Code: JOW FDA UDI
GMDN Term: Sequential venous compression system FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.5800 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size: Length — 270 Centimeter FDA UDI
Height — 150 Centimeter FDA UDI
Width — 130 Centimeter FDA UDI

Category: Sequential venous compression system

Woundexpress by Huntleigh Healthcare , Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Huntleigh Healthcare , Ltd.

Sources (1)

FDA UDI 57d48bd7-894a-4848-8243-41895eed241b 37 fields · synced May 30, 2026