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Valleylab

FDA UDI

Class II (US FDA UDI)

by Covidien LP

Identity

Trade Name
Valleylab FDA UDI
Generic Name
Electrosurgical electrode extension FDA UDI
Device Name
Straight Extension FDA UDI
Model / Reference
E1504 FDA UDI
Description
Straight Extension FDA UDI

Identifiers

Primary DI / UDI-DI
10884524001333 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrosurgical electrode extension 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

No

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
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Length — 34.3 Centimeter FDA UDI

Category: Electrosurgical electrode extension

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

Similar devices

Also classified as Electrosurgical electrode extension.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Covidien LP

Sources (1)

  • FDA UDI a97acd05-fb85-426f-b9ba-c897a1e9723e 36 fields · synced May 31, 2026