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VESALIUS STERILE single-use NON-STICK bipolar bayonet forceps

FDA UDI

Class II (US FDA UDI)

by Telea Electronic Engeenering Srl

Identity

Trade Name
VESALIUS STERILE single-use NON-STICK bipolar bayonet forceps FDA UDI
Generic Name
Open-surgery electrosurgical handpiece/electrode, bipolar, single-use FDA UDI
Model / Reference
STERILE, L=200mm T=0,25mm with cable FDA UDI

Identifiers

Catalog Number
2601034 FDA UDI
Primary DI / UDI-DI
08034055296882 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Open-surgery electrosurgical handpiece/electrode, bipolar, 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: Open-surgery electrosurgical handpiece/electrode, bipolar, single-use

VESALIUS STERILE single-use NON-STICK bipolar bayonet forceps by Telea Electronic Engeenering Srl — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Open-surgery electrosurgical handpiece/electrode, bipolar, single-use.

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 85796342-d18b-467c-8d99-65d8817aacde 33 fields · synced May 31, 2026