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Conmed

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
CONMED FDA UDI
Generic Name
Endoscopic electrosurgical electrode, bipolar, reusable FDA UDI
Device Name
BIPOLAR ELECTROSURGICAL FORCEPS, CUSHINGS 7-1/2" BAYONET MICRO-TIP FDA UDI
Model / Reference
60-1769-001 FDA UDI
Description
BIPOLAR ELECTROSURGICAL FORCEPS, CUSHINGS 7-1/2" BAYONET MICRO-TIP FDA UDI

Identifiers

Catalog Number
60-1769-001 FDA UDI
Primary DI / UDI-DI
20653405008825 FDA UDI
510(k) Number
K964176 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Endoscopic electrosurgical electrode, bipolar, 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

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Endoscopic electrosurgical electrode, bipolar, reusable

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

Similar devices

Also classified as Endoscopic electrosurgical electrode, bipolar, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 2539366b-6d11-43de-9489-390814acdad1 37 fields · synced Jun 8, 2026