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Trojan Raw - Non Latex

FDA UDI

Class II (US FDA UDI)

by Church & Dwight Co., Inc.

Identity

Trade Name
Trojan Raw - Non Latex FDA UDI
Generic Name
Basic male condom, synthetic polymer FDA UDI
Device Name
For Contraception Plus STI Protection FDA UDI
Model / Reference
00022600999836 FDA UDI
Description
For Contraception Plus STI Protection FDA UDI

Identifiers

Primary DI / UDI-DI
00022600999836 FDA UDI
510(k) Number
K203541 FDA UDI
FDA Product Code
MOL FDA UDI
GMDN Term
Basic male condom, synthetic polymer 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

No

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, synthetic polymer

Trojan Raw - Non Latex by Church & Dwight Co., Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic male condom, synthetic polymer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Church & Dwight Co., Inc.

Sources (1)

  • FDA UDI d54cc344-69f8-48c7-8780-01d9609cd110 35 fields · synced Jun 9, 2026