← Back to catalogue

Millennium

FDA UDI

Class II (US FDA UDI)

by AVALIGN TECHNOLOGIES, Inc.

Identity

Trade Name
Millennium FDA UDI
Generic Name
Low-pressure tubing connector, reusable FDA UDI
Device Name
PREMIUM SUCTION TUBING 3/8 X 10' FDA UDI
Model / Reference
39-B1540 FDA UDI
Description
PREMIUM SUCTION TUBING 3/8 X 10' FDA UDI

Identifiers

Primary DI / UDI-DI
00190776154417 FDA UDI
FDA Product Code
GAZ FDA UDI
GMDN Term
Low-pressure tubing connector, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6740 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

Yes

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: Low-pressure tubing connector, reusable

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

Similar devices

Also classified as Low-pressure tubing connector, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
AVALIGN TECHNOLOGIES, Inc.

Sources (1)

  • FDA UDI f4edba48-104a-43f3-b0fc-b4738537efb0 34 fields · synced May 31, 2026