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Valleylab

FDA UDI

Class II (US FDA UDI)

by Covidien LP

Identity

Trade Name
Valleylab FDA UDI
Generic Name
Electrosurgical return electrode, single-use FDA UDI
Device Name
REM Polyhesive (TM) Adult Cordless Patient Return Electrode FDA UDI
Model / Reference
E7509B FDA UDI
Description
REM Polyhesive (TM) Adult Cordless Patient Return Electrode FDA UDI

Identifiers

Primary DI / UDI-DI
10884524001012 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrosurgical return electrode, single-use 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrosurgical return electrode, single-use

Valleylab by Covidien LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrosurgical return electrode, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Covidien LP

Sources (1)

  • FDA UDI 79726ed4-41c2-4bbe-a2ed-0a519d936c3e 36 fields · synced Jun 6, 2026