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Trokamed

FDA UDI

Class II (US FDA UDI)

by TROKAMED GmbH

Identity

Trade Name
Trokamed FDA UDI
Generic Name
Endoscopic electrosurgical electrode, monopolar, reusable FDA UDI
Device Name
Loop Electrode 27 Ch. angled for 30° Optic FDA UDI
Model / Reference
URE02798 FDA UDI
Description
Loop Electrode 27 Ch. angled for 30° Optic FDA UDI

Identifiers

Catalog Number
URE02798 FDA UDI
Primary DI / UDI-DI
04251303808701 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

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, monopolar, reusable

Trokamed by TROKAMED GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic electrosurgical electrode, monopolar, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
TROKAMED GmbH

Sources (1)

  • FDA UDI 9f4c8b3d-6c08-4541-8ac4-21c7fe9ab8e0 35 fields · synced May 30, 2026