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VESALIUS tungsten round loop

FDA UDI

Class II (US FDA UDI)

by Telea Electronic Engeenering Srl

Identity

Trade Name
VESALIUS tungsten round loop FDA UDI
Generic Name
Open-surgery electrosurgical electrode, monopolar, reusable FDA UDI
Model / Reference
D=0,17mm d=15mm L=100mm FDA UDI

Identifiers

Catalog Number
2603051 FDA UDI
Primary DI / UDI-DI
08034055292495 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Open-surgery 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Open-surgery electrosurgical electrode, monopolar, reusable

VESALIUS tungsten round loop by Telea Electronic Engeenering Srl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Open-surgery electrosurgical electrode, monopolar, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Telea Electronic Engeenering Srl

Sources (1)

  • FDA UDI d2987d7a-879c-4aa3-9653-6f7017c08bb7 33 fields · synced Jun 1, 2026