← Back to catalogue

ONE Vanish

FDA UDI

Class II (US FDA UDI)

by Global Protection Corp.

Identity

Trade Name
ONE Vanish FDA UDI
Generic Name
Basic male condom, Hevea-latex FDA UDI
Device Name
ONE Vanish USA Economy 3-Pack, Case of 36 (6 Bundles of 6) FDA UDI
Model / Reference
111306C FDA UDI
Description
ONE Vanish USA Economy 3-Pack, Case of 36 (6 Bundles of 6) FDA UDI

Identifiers

Primary DI / UDI-DI
20726893114962 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

ONE Vanish 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 b56bd329-672c-49e8-9f85-b71a47b79674 34 fields · synced May 30, 2026