← Back to catalogue

Vitalitec

FDA UDI

Class II (US FDA UDI)

by Vitalitec International Medizintechnik GmbH

Identity

Trade Name
Vitalitec FDA UDI
Generic Name
Open-surgery electrosurgical handpiece/electrode, bipolar, single-use FDA UDI
Device Name
Bipolar Insert fenestrated, 34 cm FDA UDI
Model / Reference
L-000703 FDA UDI
Description
Bipolar Insert fenestrated, 34 cm FDA UDI

Identifiers

Catalog Number
L-000703 FDA UDI
Primary DI / UDI-DI
04250325414280 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

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
MRI Safety
MR Unsafe FDA UDI

Category: Open-surgery electrosurgical handpiece/electrode, bipolar, single-use

Vitalitec by Vitalitec International Medizintechnik GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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

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

Manufacturer

Manufacturer
Vitalitec International Medizintechnik GmbH

Sources (1)

  • FDA UDI f1dcf347-ec36-4140-8d90-a3a74d28875a 34 fields · synced May 30, 2026