← Back to catalogue

One Vanish Hyperthin

FDA UDI

Class II (US FDA UDI)

by Global Protection Corp.

Identity

Trade Name
One Vanish Hyperthin FDA UDI
Generic Name
Basic male condom, Hevea-latex FDA UDI
Device Name
Male Lubricated Latex Condoms FDA UDI
Model / Reference
111308 FDA UDI
Description
Male Lubricated Latex Condoms FDA UDI

Identifiers

Primary DI / UDI-DI
00726893111950 FDA UDI
FDA Product Code
QRZ FDA UDI
HIS FDA UDI
GMDN Term
Basic male condom, Hevea-latex FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.5305 FDA UDI
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

One Vanish Hyperthin 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI e81cf120-3fcf-4c5d-a9ff-16c8b1c2ad9e 34 fields · synced Jun 8, 2026