← Back to catalogue

Millennium

FDA UDI

Class I (US FDA UDI)

by AVALIGN TECHNOLOGIES, Inc.

Identity

Trade Name
Millennium FDA UDI
Generic Name
Ear scissors, reusable FDA UDI
Device Name
Belucci Scissors Blade,Curved Right, BL7mm SL80mm(3 1/8"), OL 135mm(5 3/8") FDA UDI
Model / Reference
1-385206 FDA UDI
Description
Belucci Scissors Blade,Curved Right, BL7mm SL80mm(3 1/8"), OL 135mm(5 3/8") FDA UDI

Identifiers

Primary DI / UDI-DI
00190776385439 FDA UDI
FDA Product Code
LRC FDA UDI
GMDN Term
Ear scissors, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.4420 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: Ear scissors, reusable

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

Similar devices

Also classified as Ear scissors, 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

Sources (1)

  • FDA UDI b84cf98e-95de-470e-a023-9c6199464364 34 fields · synced Jun 1, 2026