← Back to catalogue

Walgreens

FDA UDI

Class II (US FDA UDI)

by Walgreen Co.

Identity

Trade Name
Walgreens FDA UDI
Generic Name
Sexual lubricant FDA UDI
Device Name
Lubricating Gel FDA UDI
Model / Reference
NS#1586G FDA UDI
Description
Lubricating Gel FDA UDI

Identifiers

Primary DI / UDI-DI
00311917202419 FDA UDI
510(k) Number
K001077 FDA UDI
FDA Product Code
NUC FDA UDI
GMDN Term
Sexual 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

Dimensions & Sizes

Size
Weight — 113 Gram FDA UDI

Category: Sexual lubricant

Walgreens by Walgreen Co. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sexual lubricant.

Cleared under the same submission

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
Walgreen Co.

Sources (1)

  • FDA UDI e060dedf-599a-49f9-817d-79c486141eba 36 fields · synced Jun 6, 2026