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VESALIUS STERILE single-use neutral insulated plate for adults

FDA UDI

Class II (US FDA UDI)

by Telea Electronic Engeenering Srl

Identity

Trade Name
VESALIUS STERILE single-use neutral insulated plate for adults FDA UDI
Generic Name
Electrosurgical return electrode, single-use, sterile FDA UDI
Model / Reference
STERILE FDA UDI

Identifiers

Catalog Number
2503002 FDA UDI
Primary DI / UDI-DI
08034055290354 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrosurgical return electrode, single-use, sterile 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: Electrosurgical return electrode, single-use, sterile

VESALIUS STERILE single-use neutral insulated plate for adults by Telea Electronic Engeenering Srl — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Electrosurgical return electrode, single-use, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cc39bcd7-c9ab-4ee4-84d6-ccdd45bf6d38 33 fields · synced Jun 8, 2026