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Vitra Multispot

FDA UDI

Class II (US FDA UDI)

by Quantel Medical

Identity

Trade Name
VITRA MULTISPOT FDA UDI
Generic Name
Ophthalmic solid-state laser system FDA UDI
Device Name
532nm Multispot Laser Retinal Photocoagulation FDA UDI
Model / Reference
VMS FDA UDI
Description
532nm Multispot Laser Retinal Photocoagulation FDA UDI

Identifiers

Primary DI / UDI-DI
03700542625415 FDA UDI
FDA Product Code
GEX FDA UDI
GMDN Term
Ophthalmic solid-state laser system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 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

No

FDA UDI

Category: Ophthalmic solid-state laser system

Vitra Multispot by Quantel Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic solid-state laser system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Quantel Medical

Sources (1)

  • FDA UDI decd9bea-50ef-4a26-8ae0-8413ae17d5e1 34 fields · synced Jun 8, 2026