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Faro

FDA UDI

Class I (US FDA UDI)

by F.a.r.o. Fabbrica Apparecchiature Razionali Odontoiatriche Spa

Identity

Trade Name
FARO FDA UDI
Generic Name
Reflective dental room light FDA UDI
Device Name
EVA PCAM TW SENS.CNUS STATIVO FDA UDI
Model / Reference
EVA FDA UDI
Description
EVA PCAM TW SENS.CNUS STATIVO FDA UDI

Identifiers

Catalog Number
5S2042001 FDA UDI
Primary DI / UDI-DI
08054320511960 FDA UDI
FDA Product Code
EAZ FDA UDI
GMDN Term
Reflective dental room light FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4630 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Reflective dental room light

Faro by F.a.r.o. Fabbrica Apparecchiature Razionali Odontoiatriche Spa — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Reflective dental room light.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
F.a.r.o. Fabbrica Apparecchiature Razionali Odontoiatriche Spa

Sources (1)

  • FDA UDI 8ecd4076-6857-46e8-98d4-ae0ca602bd9c 34 fields · synced May 30, 2026