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My One

FDA UDI

Class II (US FDA UDI)

by Global Protection Corp.

Identity

Trade Name
My One FDA UDI
Generic Name
Basic male condom, Hevea-latex FDA UDI
Device Name
My One bulk pack- 100pcs * 36 bags FDA UDI
Model / Reference
MYONE-49C FDA UDI
Description
My One bulk pack- 100pcs * 36 bags FDA UDI

Identifiers

Primary DI / UDI-DI
20726893116157 FDA UDI
FDA Product Code
HIS FDA UDI
GMDN Term
Basic male condom, Hevea-latex 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: Basic male condom, Hevea-latex

My One by Global Protection Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic male condom, Hevea-latex.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI db536afe-6b05-4deb-b60a-1f953ff34490 35 fields · synced Jun 8, 2026