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Smile Makers

FDA UDI

Class II (US FDA UDI)

by Meiyume Manufacturing (thailand) Limited

Identity

Trade Name
Smile Makers FDA UDI
Generic Name
Sexual lubricant FDA UDI
Device Name
Personal lubricant FDA UDI
Model / Reference
60 ml FDA UDI
Description
Personal lubricant FDA UDI

Identifiers

Primary DI / UDI-DI
08859350704111 FDA UDI
510(k) Number
K182100 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

No

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

Yes

FDA UDI

Category: Sexual lubricant

Smile Makers by Meiyume Manufacturing (thailand) Limited — 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

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Manufacturer

Sources (1)

  • FDA UDI 9d6eb7eb-6fe4-46be-83d7-7bdfd049a411 36 fields · synced May 30, 2026