FDA UDI In Commercial Distribution 🇺🇸 United States

DUREX Performax Intense Condom

DI: 00302340983549 · Model: Condom · RB Health (us) LLC
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
24

Basic Information

Brand Name
DUREX Performax Intense Condom
Primary DI
00302340983549
Version / Model
Condom
Company Name
RB Health (us) LLC
Labeler DUNS
081049410
Distribution Status
In Commercial Distribution
Device Count in Pkg
24
Record Status
Published
Publish Date
2019-10-30
Public Version
1
Public Version Date
2019-11-07
Public Version Status
New
Public Device Record Key
02470f43-e52d-476a-ac91-0cbf4a52aa9d

Device Description

Condom

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
Yes
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 10302340983546
Primary 00302340983549
Package 20302340983543
Unit of Use 40302340983547

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K020659 000

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