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Lumindex 3 LED Transilluminator Standard 3mm Light Guide

FDA UDI

Class I (US FDA UDI)

by Practicon, Inc.

Identity

Trade Name
Lumindex 3 LED Transilluminator Standard 3mm Light Guide FDA UDI
Generic Name
ENT transilluminator FDA UDI
Model / Reference
7118836 FDA UDI

Identifiers

Catalog Number
71-18836 FDA UDI
Primary DI / UDI-DI
00723896009079 FDA UDI
FDA Product Code
HJN FDA UDI
GMDN Term
ENT transilluminator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.1945 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: ENT transilluminator

Lumindex 3 LED Transilluminator Standard 3mm Light Guide by Practicon, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as ENT transilluminator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Practicon, Inc.

Sources (1)

  • FDA UDI 85da3f9c-e8fe-4682-8a76-44ef02713d56 33 fields · synced May 30, 2026