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Millennium

FDA UDI

Class II (US FDA UDI)

by AVALIGN TECHNOLOGIES, Inc.

Identity

Trade Name
Millennium FDA UDI
Generic Name
Arthroscopic access cannula, reusable FDA UDI
Device Name
5MM DIA., 00CM REUSABLE STAINLESS STEEL CANNULA +OBTURATOR SET CONSISTING OF: (1) OUTER CANNULA, 5MM DIA., 20CM WITH HANDLE AND LUER LOCK FITTING. (1) OBTURATOR 3.8MM DIA., 22CM WITH HANDLE AND ROUND TIP FDA UDI
Model / Reference
72-52205108 FDA UDI
Description
5MM DIA., 00CM REUSABLE STAINLESS STEEL CANNULA +OBTURATOR SET CONSISTING OF: (1) OUTER CANNULA, 5MM DIA., 20CM WITH HANDLE AND LUER LOCK FITTING. (1) OBTURATOR 3.8MM DIA., 22CM WITH HANDLE AND ROUND TIP FDA UDI

Identifiers

Primary DI / UDI-DI
00190776153649 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Arthroscopic access cannula, reusable 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: Arthroscopic access cannula, reusable

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

Similar devices

Also classified as Arthroscopic access cannula, 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 9316eed8-f61e-4a05-ad44-e9400146ed24 34 fields · synced May 30, 2026