← Back to catalogue

Beamer AVEO

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
Beamer AVEO FDA UDI
Generic Name
Argon-enhanced electrosurgical system gas delivery unit FDA UDI
Device Name
Beamer AVEO Argon Module FDA UDI
Model / Reference
AVEO-ABC FDA UDI
Description
Beamer AVEO Argon Module FDA UDI

Identifiers

Catalog Number
AVEO-ABC FDA UDI
Primary DI / UDI-DI
20845854081492 FDA UDI
510(k) Number
K214058 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Argon-enhanced electrosurgical system gas delivery unit 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Argon-enhanced electrosurgical system gas delivery unit

Beamer AVEO by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Argon-enhanced electrosurgical system gas delivery unit.

Cleared under the same submission

K214058 also covers:

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
Conmed Corporation

Sources (1)

  • FDA UDI c2476ce6-1ca3-4235-b7c4-2c6fedd1e897 37 fields · synced Jun 8, 2026