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Millennium

FDA UDI

Class II (US FDA UDI)

by AVALIGN TECHNOLOGIES, Inc.

Identity

Trade Name
Millennium FDA UDI
Generic Name
Rigid optical cystourethroscope FDA UDI
Device Name
CYSTOURETHROSCOPE BRIDGE WITH DUAL CHANNEL FDA UDI
Model / Reference
72-3140057 FDA UDI
Description
CYSTOURETHROSCOPE BRIDGE WITH DUAL CHANNEL FDA UDI

Identifiers

Primary DI / UDI-DI
00190776143787 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Rigid optical cystourethroscope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 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

No

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 cystourethroscope

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

Similar devices

Also classified as Rigid optical cystourethroscope.

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 ba8cd4ed-00c4-4b40-9f15-de87ecf93a1b 34 fields · synced May 31, 2026