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VICTUS™ Femtosecond Laser Platform

FDA UDI

Class II (US FDA UDI)

by Technolas GmbH Perfect Vision

Identity

Trade Name
VICTUS™ Femtosecond Laser Platform FDA UDI
Generic Name
Femtosecond ophthalmic solid-state laser system FDA UDI
Device Name
The laser system is an ophthalmologic system based on femtosecond technology. It is used to treat a wide variety of ophthalmologic indications. FDA UDI
Model / Reference
3.2 FDA UDI
Description
The laser system is an ophthalmologic system based on femtosecond technology. It is used to treat a wide variety of ophthalmologic indications. FDA UDI

Identifiers

Catalog Number
14000 FDA UDI
Primary DI / UDI-DI
04050555002895 FDA UDI
FDA Product Code
OOE FDA UDI
GMDN Term
Femtosecond ophthalmic solid-state laser system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4390 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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Femtosecond ophthalmic solid-state laser system

VICTUS™ Femtosecond Laser Platform by Technolas GmbH Perfect Vision — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Femtosecond ophthalmic solid-state laser system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 16b567e1-79b9-4e4a-a511-67bccb0801f5 35 fields · synced May 30, 2026