← Back to catalogue

One

FDA UDI

Class II (US FDA UDI)

by Lunamax Llc

Identity

Trade Name
ONE FDA UDI
Generic Name
Basic male condom, Hevea-latex FDA UDI
Device Name
ONE Chocolate Strawberry Flavored Latex Condom FDA UDI
Model / Reference
GS144 FDA UDI
Description
ONE Chocolate Strawberry Flavored Latex Condom FDA UDI

Identifiers

Primary DI / UDI-DI
00850002174731 FDA UDI
510(k) Number
K024324 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

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

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 by Lunamax Llc — 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

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

Manufacturer

Manufacturer
Lunamax Llc

Sources (1)

  • FDA UDI a6a91e0c-eb96-4302-84a1-eb58303d1d71 34 fields · synced Jun 1, 2026