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MyONE Super Wide D22/64J

FDA UDI

Class II (US FDA UDI)

by Global Protection Corp.

Identity

Trade Name
MyONE Super Wide D22/64J FDA UDI
Generic Name
Basic male condom, Hevea-latex FDA UDI
Device Name
10 Lubricated Latex Condoms FDA UDI
Model / Reference
MYTD22/64J-10 FDA UDI
Description
10 Lubricated Latex Condoms FDA UDI

Identifiers

Primary DI / UDI-DI
00726893114418 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

MyONE Super Wide D22/64J 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 d9d0734d-b8c7-48ee-ad4d-46ac2e14a16d 33 fields · synced May 30, 2026