FDA UDI In Commercial Distribution 🇺🇸 United States

SKYN

DI: 08859798106041 · Model: 08859798106041 · SURETEX LIMITED - BRANCH
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
16

Basic Information

Brand Name
SKYN
Primary DI
08859798106041
Version / Model
08859798106041
Company Name
SURETEX LIMITED - BRANCH
Labeler DUNS
672044515
Distribution Status
In Commercial Distribution
Device Count in Pkg
16
Record Status
Published
Publish Date
2025-06-18
Public Version
1
Public Version Date
2025-06-26
Public Version Status
New
Public Device Record Key
999f1d7d-8723-4873-b020-5ff48f47e461

Device Description

SKYN Supreme Feel Non-Latex Condom BX16 CA RP

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
Yes

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
Unit of Use 28859798106045
Primary 08859798106041

Premarket Submissions

Submission Number Supplement Number
K231908 000