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Millennium

FDA UDI

Class I (US FDA UDI)

by AVALIGN TECHNOLOGIES, Inc.

Identity

Trade Name
Millennium FDA UDI
Generic Name
ENT speculum holder FDA UDI
Device Name
Bottom portion of the toggle clamp assembly, adaptor (knurled piece), red rubber washer, a cradle and a screw (holds these together) for Tobey Laryngoscope 92-500248, FDA UDI
Model / Reference
92-48TOGGLEB FDA UDI
Description
Bottom portion of the toggle clamp assembly, adaptor (knurled piece), red rubber washer, a cradle and a screw (holds these together) for Tobey Laryngoscope 92-500248, FDA UDI

Identifiers

Primary DI / UDI-DI
00190776405175 FDA UDI
FDA Product Code
CCW FDA UDI
GMDN Term
ENT speculum holder FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5540 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

No

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: ENT speculum holder

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

Similar devices

Also classified as ENT speculum holder.

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 4ac9804d-d467-4d16-a9f7-c06e9d2bedd4 34 fields · synced Jun 1, 2026