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ID Millennium

FDA UDI

Class II (US FDA UDI)

by Westridge Laboratories Incorporated

Identity

Trade Name
ID Millennium FDA UDI
Generic Name
Vaginal lubricant FDA UDI
Device Name
ID Millennium is a Silicone based lubricant, and is Latex Compatible. FDA UDI
Model / Reference
Millennium 12 ml Tube FDA UDI
Description
ID Millennium is a Silicone based lubricant, and is Latex Compatible. FDA UDI

Identifiers

Catalog Number
IDDMIT10 FDA UDI
Primary DI / UDI-DI
00761236109928 FDA UDI
510(k) Number
K141767 FDA UDI
FDA Product Code
NUC FDA UDI
GMDN Term
Vaginal lubricant FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.5300 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vaginal lubricant

ID Millennium by Westridge Laboratories Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vaginal lubricant.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bd9903cc-6419-4212-98b3-765a1e3b9ced 36 fields · synced May 30, 2026