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Abc

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
ABC FDA UDI
Generic Name
Inert gas-enhanced endoscopic electrosurgical electrode, single-use FDA UDI
Device Name
ABC PROBE 5 MM FOOTSWITCHING PROBE FDA UDI
Model / Reference
160655 FDA UDI
Description
ABC PROBE 5 MM FOOTSWITCHING PROBE FDA UDI

Identifiers

Catalog Number
160655 FDA UDI
Primary DI / UDI-DI
10653405003885 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

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

Abc 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.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 90af6fd3-d1a6-4cfc-9eb8-47c596396831 36 fields · synced May 30, 2026