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überlube

FDA UDI

Class II (US FDA UDI)

by Uberlube

Identity

Trade Name
überlube FDA UDI
Generic Name
Sexual lubricant FDA UDI
Device Name
Good-To-Go Refills + Refills FDA UDI
Model / Reference
UBER-30RF+30RF FDA UDI
Description
Good-To-Go Refills + Refills FDA UDI

Identifiers

Catalog Number
UBER-30RF+30RF FDA UDI
Primary DI / UDI-DI
00851674003114 FDA UDI
510(k) Number
K151647 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
Not 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

überlube by Uberlube — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K151647 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Uberlube

Sources (1)

  • FDA UDI 1bc1843a-9cd6-40b0-90d7-66ede57a4469 36 fields · synced Jun 8, 2026