Ligasure

FDA UDI

Class II (US FDA UDI)

by Covidien LP

Identity

Trade Name: Ligasure FDA UDI
Generic Name: Foot-switch, electrical FDA UDI
Device Name: Tissue Fusion Footswitch, Orange FDA UDI
Model / Reference: LF0500 FDA UDI
Description: Tissue Fusion Footswitch, Orange FDA UDI

Identifiers

Primary DI / UDI-DI: 10884524001678 FDA UDI
510(k) Number: K051644 FDA UDI
FDA Product Code: GEI FDA UDI
GMDN Term: Foot-switch, electrical FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 878.4400 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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Foot-switch, electrical

Ligasure by Covidien LP — 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: Covidien LP

Sources (1)

FDA UDI c9faabe3-8ffc-4acb-a1d4-3dfb9b4dd760 36 fields · synced May 30, 2026