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Millennium

FDA UDI

Class I (US FDA UDI)

by AVALIGN TECHNOLOGIES, Inc.

Identity

Trade Name
Millennium FDA UDI
Generic Name
Rigid optical laryngopharyngoscope FDA UDI
Device Name
Light carrier for Ossoff Adult laryngoscope light carrier and cable with Pilling adapter FDA UDI
Model / Reference
72-407860 FDA UDI
Description
Light carrier for Ossoff Adult laryngoscope light carrier and cable with Pilling adapter FDA UDI

Identifiers

Primary DI / UDI-DI
00190776189105 FDA UDI
FDA Product Code
CCW FDA UDI
GMDN Term
Rigid optical laryngopharyngoscope FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5540 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

Yes

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: Rigid optical laryngopharyngoscope

Millennium by AVALIGN TECHNOLOGIES, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Rigid optical laryngopharyngoscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
AVALIGN TECHNOLOGIES, Inc.

Sources (1)

  • FDA UDI 49f46ae2-d05c-44fa-82b8-3933adb605c4 34 fields · synced Jun 8, 2026