← Back to catalogue

VESALIUS STERILE single-use endoscopic probe for ablation

FDA UDI

Class II (US FDA UDI)

by Telea Electronic Engeenering Srl

Identity

Trade Name
VESALIUS STERILE single-use endoscopic probe for ablation FDA UDI
Generic Name
Percutaneous radio-frequency ablation probe, denervation, monopolar, single-use FDA UDI
Model / Reference
STERILE FDA UDI

Identifiers

Catalog Number
2610004 FDA UDI
Primary DI / UDI-DI
08034055293850 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Percutaneous radio-frequency ablation probe, denervation, monopolar, single-use 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

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

Category: Percutaneous radio-frequency ablation probe, denervation, monopolar, single-use

VESALIUS STERILE single-use endoscopic probe for ablation by Telea Electronic Engeenering Srl — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Percutaneous radio-frequency ablation probe, denervation, monopolar, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Telea Electronic Engeenering Srl

Sources (1)

  • FDA UDI b19b5d21-e62d-4d0b-8bc9-2563c0d7a55e 33 fields · synced May 30, 2026