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Equaline

FDA UDI

Class II (US FDA UDI)

by Supervalu Inc.

Identity

Trade Name
Equaline FDA UDI
Generic Name
Vaginal lubricant FDA UDI
Device Name
Personal Lubricant 4oz. (113g) FDA UDI
Model / Reference
7W926ELC2 FDA UDI
Description
Personal Lubricant 4oz. (113g) FDA UDI

Identifiers

Primary DI / UDI-DI
00041163250925 FDA UDI
510(k) Number
K180923 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vaginal lubricant

Equaline by Supervalu Inc. — 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

Manufacturer
Supervalu Inc.

Sources (1)

  • FDA UDI 98e41749-925a-4abb-915d-f8ea30744c3a 34 fields · synced May 31, 2026