FDA UDI In Commercial Distribution 🇺🇸 United States

DUREX® Pleasure Pack

DI: 00302340300421 · Model: 00302340300421 · RB Health (us) LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
3

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
DUREX® Pleasure Pack
Primary DI
00302340300421
Version / Model
00302340300421
Company Name
RB Health (us) LLC
Labeler DUNS
081049410
Distribution Status
In Commercial Distribution
Device Count in Pkg
3
Record Status
Published
Publish Date
2025-03-20
Public Version
2
Public Version Date
2025-05-05
Public Version Status
Update
Public Device Record Key
5ca03f71-eeda-43f4-a3eb-14ff06f52f1e

Device Description

Durex Pleasure Pack Condom - 3ct. Contains: Extra Sensitive Thin - 1ct. Extra Sensitive Stimulating - 1ct. Performax Intense - 1ct.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
Yes
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HIS Condom

GMDN Terms

Code Name
45138 Basic male condom, Hevea-latex

Identifiers

Type ID
Package 00302340300490
Primary 00302340300421
Unit of Use 99302340300425

Customer Contacts

Storage Conditions

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