Millennium

FDA UDI

Class I (US FDA UDI)

by AVALIGN TECHNOLOGIES, Inc.

Identity

Trade Name: MILLENNIUM FDA UDI
Generic Name: Corneoscleral punch FDA UDI
Device Name: Troutman Corneal Punch FDA UDI
Model / Reference: 85-71002928 FDA UDI
Description: Troutman Corneal Punch FDA UDI

Identifiers

Primary DI / UDI-DI: 00190776374006 FDA UDI
FDA Product Code: HNJ FDA UDI
GMDN Term: Corneoscleral punch FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 886.4350 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: Corneoscleral punch

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

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ATLAS — ATLAS CERRAHİ ALETLER LTD. ŞTİ. · Class I
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Corneal Trephine Handle Ø 7.5 mm Stainless Steel — SURTEX INSTRUMENTS LTD · 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

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Manufacturer

Manufacturer: AVALIGN TECHNOLOGIES, Inc.

Sources (1)

FDA UDI 01f0372d-28c3-4587-ad80-21a8351bb242 34 fields · synced May 29, 2026