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Cefla

FDA UDI

Class I (US FDA UDI)

by Cefla Societa' Cooperativa

Identity

Trade Name
CEFLA FDA UDI
Generic Name
Reflective dental room light FDA UDI
Device Name
The device is a dental operating light intended to illuminate oral structures and operating areas during dental treatment. FDA UDI
Model / Reference
VENUS PLUS FDA UDI
Description
The device is a dental operating light intended to illuminate oral structures and operating areas during dental treatment. FDA UDI

Identifiers

Catalog Number
96601030 FDA UDI
Primary DI / UDI-DI
08033837937494 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

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: Reflective dental room light

Cefla by Cefla Societa' Cooperativa — 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
Cefla Societa' Cooperativa

Sources (1)

  • FDA UDI 68094cc3-2505-413a-b309-bb4cff4a2371 35 fields · synced Jun 1, 2026