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Elmed

FDA UDI

Class II (US FDA UDI)

by Elmed Incorporated

Identity

Trade Name
ELMED FDA UDI
Generic Name
Electrosurgical return electrode, single-use, sterile FDA UDI
Device Name
ELMED DISPOSABLE PATIENT PLATES, SELF-ADHESIVE, PACKAGE OF 20, 4.69" X 5.06" (12CM X 13CM) FDA UDI
Model / Reference
5395 FDA UDI
Description
ELMED DISPOSABLE PATIENT PLATES, SELF-ADHESIVE, PACKAGE OF 20, 4.69" X 5.06" (12CM X 13CM) FDA UDI

Identifiers

Catalog Number
5395 FDA UDI
Primary DI / UDI-DI
00842180106116 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrosurgical return electrode, single-use, sterile 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

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electrosurgical return electrode, single-use, sterile

Elmed by Elmed Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrosurgical return electrode, single-use, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Elmed Incorporated

Sources (1)

  • FDA UDI 8a668e1a-2750-446d-930f-896a417f902a 35 fields · synced May 31, 2026