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LuxOR Revalia

FDA UDI

Class I (US FDA UDI)

by Alcon Laboratories, Inc.

Identity

Trade Name
LuxOR Revalia FDA UDI
Generic Name
Ophthalmic surgical microscope FDA UDI
Device Name
Surgical Microscope FDA UDI
Model / Reference
00380657530731 FDA UDI
Description
Surgical Microscope FDA UDI

Identifiers

Primary DI / UDI-DI
00380657530731 FDA UDI
FDA Product Code
HRM FDA UDI
GMDN Term
Ophthalmic surgical microscope FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4700 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ophthalmic surgical microscope

LuxOR Revalia by Alcon Laboratories, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic surgical microscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4bb97302-e91c-49c1-a6de-979e7ca1e95a 33 fields · synced Jun 1, 2026