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Conmed

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
CONMED FDA UDI
Generic Name
Electrosurgical handpiece/electrode holder, single-use FDA UDI
Device Name
American Dilator, Reusable, 42F FDA UDI
Model / Reference
000277 FDA UDI
Description
American Dilator, Reusable, 42F FDA UDI

Identifiers

Catalog Number
000277 FDA UDI
Primary DI / UDI-DI
10653405050766 FDA UDI
FDA Product Code
KNQ FDA UDI
GMDN Term
Electrosurgical handpiece/electrode holder, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5365 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

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrosurgical handpiece/electrode holder, single-use

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

Similar devices

Also classified as Electrosurgical handpiece/electrode holder, 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 ccbe9bed-0bda-4f29-a8f5-1bef69b321d7 35 fields · synced Jun 8, 2026