← Back to catalogue

Aveo

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
AVEO FDA UDI
Generic Name
Inert gas-enhanced endoscopic electrosurgical electrode, single-use FDA UDI
Device Name
BEAMER AVEO ARGON PROBE FILTER INTEGRATED ARGON PROBE, 1.8 MM X 160 CM FDA UDI
Model / Reference
FIA-AVEO-1 FDA UDI
Description
BEAMER AVEO ARGON PROBE FILTER INTEGRATED ARGON PROBE, 1.8 MM X 160 CM FDA UDI

Identifiers

Catalog Number
FIA-AVEO-1 FDA UDI
Primary DI / UDI-DI
20653405987205 FDA UDI
510(k) Number
K221945 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
Sterilization Method
Ethylene Oxide FDA UDI

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

Aveo by Conmed Corporation — 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.

Cleared under the same submission

K221945 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 a314e3f5-5941-415e-9222-e8be3693663a 37 fields · synced May 31, 2026