Millennium

FDA UDI

Class I (US FDA UDI)

by AVALIGN TECHNOLOGIES, Inc.

Identity

Trade Name: MILLENNIUM FDA UDI
Generic Name: ENT elevator FDA UDI
Device Name: Cottle Skin Elevator, FDA UDI
Model / Reference: 2-4650 FDA UDI
Description: Cottle Skin Elevator, FDA UDI

Identifiers

Primary DI / UDI-DI: 00190776323196 FDA UDI
FDA Product Code: KAD FDA UDI
GMDN Term: ENT elevator 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: ENT elevator

A comprehensive medical device directory featuring the Millennium ENT Elevator. Learn about its features, compliance, and FAQs.

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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

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Manufacturer

Manufacturer: AVALIGN TECHNOLOGIES, Inc.

Sources (1)

FDA UDI 0d2c9b9b-96bc-4095-9e64-489e3227389a 34 fields · synced Jul 22, 2026