← Back to catalogue

Valleylab

FDA UDI

Class II (US FDA UDI)

by Covidien LP

Identity

Trade Name
Valleylab FDA UDI
Generic Name
Inert gas-enhanced endoscopic electrosurgical electrode, single-use FDA UDI
Device Name
Laparoscopic Argon Blunt Needle Electrode Retractable FDA UDI
Model / Reference
E3583-28 FDA UDI
Description
Laparoscopic Argon Blunt Needle Electrode Retractable FDA UDI

Identifiers

Primary DI / UDI-DI
10884521767959 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Inert gas-enhanced endoscopic electrosurgical 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

Yes

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

Dimensions & Sizes

Size
Length — 28 Centimeter FDA UDI

Category: Inert gas-enhanced endoscopic electrosurgical electrode, single-use

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

Similar devices

Also classified as Inert gas-enhanced endoscopic electrosurgical electrode, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Covidien LP

Sources (1)

  • FDA UDI 2f543c49-05ba-473e-9df9-cc4195089902 36 fields · synced May 30, 2026