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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 endoscopic scissors, reusable FDA UDI
Device Name
Hook Scissors 5mm 36cm single action, insulated shaft & carbon fiber handle with RFpost, non-ratchet (type 5), modular, 3-piece screw-apart FDA UDI
Model / Reference
72-5223660C5 FDA UDI
Description
Hook Scissors 5mm 36cm single action, insulated shaft & carbon fiber handle with RFpost, non-ratchet (type 5), modular, 3-piece screw-apart FDA UDI

Identifiers

Primary DI / UDI-DI
00190776158460 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Rigid endoscopic scissors, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 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 endoscopic scissors, reusable

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

Similar devices

Also classified as Rigid endoscopic scissors, reusable.

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 13810c24-40d5-4ec1-804d-24da05b926d7 34 fields · synced May 30, 2026