Millennium

FDA UDI

Class I (US FDA UDI)

by AVALIGN TECHNOLOGIES, Inc.

Identity

Trade Name: Millennium FDA UDI
Generic Name: General/plastic surgery mirror FDA UDI
Device Name: LARYNGEAL MIRROR WHANDLE DIAMETER FDA UDI
Model / Reference: 1-460106 FDA UDI
Description: LARYNGEAL MIRROR WHANDLE DIAMETER FDA UDI

Identifiers

Primary DI / UDI-DI: 00190776184339 FDA UDI
FDA Product Code: KAI FDA UDI
GMDN Term: General/plastic surgery mirror FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 874.4420 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: General/plastic surgery mirror

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

Similar devices

Also classified as General/plastic surgery mirror.

Integra® Jarit® — Integra LifeSciences Production Corporation · Class I
V. Mueller — STERIS CORPORATION · Class I
Mirror, round, 6 mm, polished — Spiggle & Theis Medizintechnik GmbH · Class I
Symmetry Hardy — SYMMETRY SURGICAL INC. · Class I
Mirror, round, polished — Spiggle & Theis Medizintechnik GmbH · Class I
Atticus mirror — Spiggle & Theis Medizintechnik GmbH · Class I
ProneView — DUPACO, INC. · Class I
Integra® Ruggles®-Redmond™ — Integra LifeSciences Production Corporation · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: AVALIGN TECHNOLOGIES, Inc.

Sources (1)

FDA UDI d631df51-e0c4-4843-a28a-66d3ad290958 34 fields · synced May 30, 2026