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ID Condoms

FDA UDI

Class II (US FDA UDI)

by Westridge Laboratories Incorporated

Identity

Trade Name
ID Condoms FDA UDI
Generic Name
Basic male condom, Hevea-latex FDA UDI
Device Name
A premium lubricated latex condom FDA UDI
Model / Reference
ID Extra Thin (Case/1000) FDA UDI
Description
A premium lubricated latex condom FDA UDI

Identifiers

Catalog Number
IDDCNDXT FDA UDI
Primary DI / UDI-DI
10761236110280 FDA UDI
510(k) Number
K910284 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

ID Condoms by Westridge Laboratories Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic male condom, Hevea-latex.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ac2b032e-4b69-408e-9e91-0b8490546c25 36 fields · synced Jun 1, 2026