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Eliminator

FDA UDIEUDAMED

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
ELIMINATOR FDA UDI
Generic Name
Electrosurgical handpiece/electrode holder, single-use FDA UDI
Device Name
CONMED ELIMINATOR 3-Stage Esophageal PET Balloon Dilator, 15 mm x 8 cm, 45F FDA UDI
Model / Reference
000735 FDA UDI
Description
CONMED ELIMINATOR 3-Stage Esophageal PET Balloon Dilator, 15 mm x 8 cm, 45F FDA UDI

Identifiers

Catalog Number
000735 FDA UDI
Primary DI / UDI-DI
20653405052491 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

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
Catheter Gauge — 45 French FDA UDI
Length — 8 Centimeter FDA UDI
Outer Diameter — 15 Millimeter FDA UDI

Category: Electrosurgical handpiece/electrode holder, single-use

Eliminator by Conmed Corporation — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Electrosurgical handpiece/electrode holder, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (2)

  • FDA UDI d28cbcf5-6539-4095-b559-2b3251a38dbf 36 fields · synced Jun 19, 2026
  • EUDAMED 1 fields · synced May 29, 2026