DUREX® Adventure Pack

GUDID 50302340995691

Durex Adventure Pack Condom - 144ct. Contains: Extra Sensitive Smooth - 48ct. Extra Sensitive Stimulating - 48ct. Performax Intense - 48ct.

RB Health (us) LLC

Basic male condom, Hevea-latex
Primary Device ID50302340995691
NIH Device Record Key57ced7c9-6dc5-4221-b6e1-69654c4f8e5f
Commercial Distribution StatusIn Commercial Distribution
Brand NameDUREX® Adventure Pack
Version Model Number00302340995696
Company DUNS081049410
Company NameRB Health (us) LLC
Device Count144
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latextrue
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Customer Support Contacts

Phone+1(800)756-5488
Emailxxx@xxx.xxx
Phone+1(800)756-5488
Emailxxx@xxx.xxx
Phone+1(800)756-5488
Emailxxx@xxx.xxx
Phone+1(800)756-5488
Emailxxx@xxx.xxx
Phone+1(800)756-5488
Emailxxx@xxx.xxx
Phone+1(800)756-5488
Emailxxx@xxx.xxx
Phone+1(800)756-5488
Emailxxx@xxx.xxx
Phone+1(800)756-5488
Emailxxx@xxx.xxx
Phone+1(800)756-5488
Emailxxx@xxx.xxx
Phone+1(800)756-5488
Emailxxx@xxx.xxx
Phone+1(800)756-5488
Emailxxx@xxx.xxx
Phone+1(800)756-5488
Emailxxx@xxx.xxx
Phone+1(800)756-5488
Emailxxx@xxx.xxx
Phone+1(800)756-5488
Emailxxx@xxx.xxx
Phone+1(800)756-5488
Emailxxx@xxx.xxx

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place (below 100 F) and avoid exposure to direct sunlight. Avoid excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place (below 100 F) and avoid exposure to direct sunlight. Avoid excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place (below 100 F) and avoid exposure to direct sunlight. Avoid excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place (below 100 F) and avoid exposure to direct sunlight. Avoid excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place (below 100 F) and avoid exposure to direct sunlight. Avoid excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place (below 100 F) and avoid exposure to direct sunlight. Avoid excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place (below 100 F) and avoid exposure to direct sunlight. Avoid excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place (below 100 F) and avoid exposure to direct sunlight. Avoid excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place (below 100 F) and avoid exposure to direct sunlight. Avoid excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place (below 100 F) and avoid exposure to direct sunlight. Avoid excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place (below 100 F) and avoid exposure to direct sunlight. Avoid excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place (below 100 F) and avoid exposure to direct sunlight. Avoid excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place (below 100 F) and avoid exposure to direct sunlight. Avoid excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place (below 100 F) and avoid exposure to direct sunlight. Avoid excess heat
Special Storage Condition, SpecifyBetween 0 and 0 *Store in a cool dry place (below 100 F) and avoid exposure to direct sunlight. Avoid excess heat

Device Identifiers

Device Issuing AgencyDevice ID
GS100302340995696 [Primary]
GS150302340995691 [Package]
Contains: 00302340995696
Package: Case [6 Units]
In Commercial Distribution
GS199302340995690 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HISCondom

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-03-28
Device Publish Date2025-03-20

Devices Manufactured by RB Health (us) LLC

00302340300490 - DUREX® Pleasure Pack2025-03-28 Durex Pleasure Pack Condom - 3ct. Contains: Extra Sensitive Thin - 1ct. Extra Sensitive Stimulating - 1ct. Performax Intense -
50302340989331 - DUREX® Pleasure Pack2025-03-28 Durex Pleasure Pack Condom - 42ct. Contains: Extra Sensitive Thin - 11ct. Extra Sensitive Smooth - 10ct. Extra Sensitive Stimul
50302340995691 - DUREX® Adventure Pack2025-03-28Durex Adventure Pack Condom - 144ct. Contains: Extra Sensitive Smooth - 48ct. Extra Sensitive Stimulating - 48ct. Performax Intense - 48ct.
50302340995691 - DUREX® Adventure Pack2025-03-28 Durex Adventure Pack Condom - 144ct. Contains: Extra Sensitive Smooth - 48ct. Extra Sensitive Stimulating - 48ct. Performax Int
10067981087984 - DUREX® Air Regular Fit; DUREX® Air 2025-03-21 Durex Air Regular Fit Condom 10ct. Durex Air Condom 10ct.
50302340876570 - DUREX® Air Regular Fit; DUREX® Air 2025-03-21 Durex Air Regular Fit Condom 36ct. Durex Air Condom 36ct.
20302340090005 - DUREX Tropical Condoms2025-03-21 DUREX Tropical Condoms 3ct.
50302340129003 - DUREX Extra Sensitive Condom2025-03-21 Extra Sensitive Thin Condom 3ct. Extra Sensitive Thin Regular Fit 3ct.
50302340876600 - DUREX Extra Sensitive Condom2025-03-21 Extra Sensitive Thin Condom 24ct. Extra Sensitive Thin Regular Fit 24ct.

Trademark Results [DUREX]

Mark Image

Registration | Serial
Company
Trademark
Application Date
DUREX
DUREX
97515518 not registered Live/Pending
LRC Products Limited
2022-07-22
DUREX
DUREX
88508058 not registered Live/Pending
DURABOND PRODUCTS LIMITED
2019-07-10
DUREX
DUREX
88175799 not registered Live/Pending
LRC Products Limited
2018-10-31
DUREX
DUREX
85743366 not registered Dead/Abandoned
LRC Products Limited
2012-10-02
DUREX
DUREX
85740902 4900035 Live/Registered
LRC Products Limited
2012-09-28
DUREX
DUREX
85369151 4971250 Live/Registered
LRC Products Limited
2011-07-12
DUREX
DUREX
80986035 0986035 Dead/Cancelled
LRC International Limited
0000-00-00
DUREX
DUREX
79334893 not registered Live/Pending
LRC Products Limited
2021-12-14
DUREX
DUREX
79256491 5917374 Live/Registered
LRC Products Limited
2019-03-07
DUREX
DUREX
78651988 3176354 Live/Registered
HAJ, Inc.
2005-06-16
DUREX
DUREX
78247431 3179168 Dead/Cancelled
LRC Products Limited
2003-05-08
DUREX
DUREX
76613733 3039455 Live/Registered
PALMER ASPHALT COMPANY
2004-09-27

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