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One

FDA UDI

Class II (US FDA UDI)

by Global Protection Corp.

Identity

Trade Name
ONE FDA UDI
Generic Name
Sexual lubricant FDA UDI
Device Name
FC2@Home Mailer w/Oasis FDA UDI
Model / Reference
110100U-FO FDA UDI
Description
FC2@Home Mailer w/Oasis FDA UDI

Identifiers

Primary DI / UDI-DI
00726893118300 FDA UDI
FDA Product Code
HIS FDA UDI
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

Yes

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

Category: Sexual lubricant

One by Global Protection Corp. — 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 1146c0b3-29b7-446b-9491-17d6c138703d 35 fields · synced Jun 8, 2026