FDA UDI In Commercial Distribution 🇺🇸 United States

Durex Intense XL

DI: 00302340995825 · Model: 00302340995825 · RB Health (us) LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

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Basic Information

Brand Name
Durex Intense XL
Primary DI
00302340995825
Version / Model
00302340995825
Company Name
RB Health (us) LLC
Labeler DUNS
081049410
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2025-09-01
Public Version
1
Public Version Date
2025-09-09
Public Version Status
New
Public Device Record Key
da42150c-8281-4ec6-996b-25cbde8b1843

Device Description

10 ct. Durex Intense XL Nitrile Condom

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
MOL Condom, Synthetic

GMDN Terms

Code Name
34151 Basic male condom, synthetic polymer

Identifiers

Type ID
Package 00302340995931
Primary 00302340995825
Unit of Use 99302340995997

Premarket Submissions

Submission Number Supplement Number
K243967 000