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DetachaTip

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
DetachaTip FDA UDI
Generic Name
Endoscopic electrosurgical electrode, monopolar, reusable FDA UDI
Device Name
DETACHATIP III SHAFT, 5MM X 33CM MULTIPLE USE DISSECTOR, RIGHT ANGLE MEEKER FDA UDI
Model / Reference
3-1017 FDA UDI
Description
DETACHATIP III SHAFT, 5MM X 33CM MULTIPLE USE DISSECTOR, RIGHT ANGLE MEEKER FDA UDI

Identifiers

Catalog Number
3-1017 FDA UDI
Primary DI / UDI-DI
30653405061629 FDA UDI
510(k) Number
K123260 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Endoscopic electrosurgical electrode, monopolar, reusable 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Length — 33 Centimeter FDA UDI
Width — 5 Millimeter FDA UDI

Category: Endoscopic electrosurgical electrode, monopolar, reusable

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

Similar devices

Also classified as Endoscopic electrosurgical electrode, monopolar, reusable.

Cleared under the same submission

K123260 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI cc2d89c2-1e28-4b8a-b025-ef054dde9d6d 38 fields · synced Jun 8, 2026