Epimed

FDA UDI

Class II (US FDA UDI)

by Epimed International, Inc

Identity

Trade Name: Epimed FDA UDI
Generic Name: Electrosurgical return electrode, single-use FDA UDI
Device Name: Grounding Pad, 4" x 8" FDA UDI
Model / Reference: 290-GP FDA UDI
Description: Grounding Pad, 4" x 8" FDA UDI

Identifiers

Catalog Number: 290-GP FDA UDI
Primary DI / UDI-DI: 00818788022974 FDA UDI
FDA Product Code: GXY FDA UDI
GMDN Term: Electrosurgical return electrode, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 882.1320 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Dimensions & Sizes

Size: Length — 8 Inch FDA UDI
Width — 4 Inch FDA UDI

Category: Electrosurgical return electrode, single-use

Epimed by Epimed International, Inc — 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: Epimed International, Inc

Sources (1)

FDA UDI 519793b7-d173-4e44-83eb-7222dbad80bc 37 fields · synced Jun 8, 2026