← Back to catalogue

Kimono Swirl

FDA UDI

Class II (US FDA UDI)

by Mayer Laboratories

Identity

Trade Name
Kimono Swirl FDA UDI
Generic Name
Sexual lubricant FDA UDI
Device Name
Natural Personal Lubricant 3 ml FDA UDI
Model / Reference
Swirl Natural Lubricant FDA UDI
Description
Natural Personal Lubricant 3 ml FDA UDI

Identifiers

Catalog Number
54005 FDA UDI
Primary DI / UDI-DI
00016169540059 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

Yes

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

Dimensions & Sizes

Size
Total Volume — 3 Milliliter FDA UDI

Category: Sexual lubricant

Kimono Swirl by Mayer Laboratories — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sexual lubricant.

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
Mayer Laboratories

Sources (1)

  • FDA UDI 120c2cfa-3423-4ca6-b249-040ea49cdfb9 37 fields · synced May 30, 2026