← Back to catalogue

Lifestyles

FDA UDI

Class II (US FDA UDI)

by Suretex Limited - Branch

Identity

Trade Name
LIFESTYLES FDA UDI
Generic Name
Basic male condom, synthetic polymer FDA UDI
Device Name
LIFESTYLES PLEASURE COLLECTION 36CT (CONTAINS: SKYN ELITE, SKYN ORIGINAL, ULTRA SENSITIVE PLATINUM, ULTRA SENSITIVE AND ASSORTED FLAVORS) FDA UDI
Model / Reference
3000 FDA UDI
Description
LIFESTYLES PLEASURE COLLECTION 36CT (CONTAINS: SKYN ELITE, SKYN ORIGINAL, ULTRA SENSITIVE PLATINUM, ULTRA SENSITIVE AND ASSORTED FLAVORS) FDA UDI

Identifiers

Primary DI / UDI-DI
00070907030004 FDA UDI
510(k) Number
K000408 FDA UDI
K160399 FDA UDI
K163107 FDA UDI
K941258 FDA UDI
FDA Product Code
MOL FDA UDI
HIS 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

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-latexBasic male condom, synthetic polymer

Lifestyles by Suretex Limited - Branch — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Basic male condom, synthetic polymer.

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

Sources (1)

  • FDA UDI 633051d7-d313-447b-92a1-d95f40cf0533 34 fields · synced Jun 1, 2026