FDA UDI In Commercial Distribution 🇺🇸 United States

SKYN

DI: 00070907000182 · Model: 0018 · SURETEX LIMITED - BRANCH
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
24

Basic Information

Brand Name
SKYN
Primary DI
00070907000182
Version / Model
0018
Company Name
SURETEX LIMITED - BRANCH
Labeler DUNS
672044515
Distribution Status
In Commercial Distribution
Device Count in Pkg
24
Record Status
Published
Publish Date
2021-08-19
Public Version
4
Public Version Date
2023-07-26
Public Version Status
Update
Public Device Record Key
d3efbe39-d32e-4bd5-adbf-b0da9c672a82

Device Description

SKYN SELECTION 24CT (ORIGINAL, EXCITATION, ELITE EXTRA LUBE & ELITE)

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
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 10070907000189
Primary 00070907000182
Package 30070907000183
Unit of Use 80070907101397

Customer Contacts

Phone
848-229-3224

Premarket Submissions

Submission Number Supplement Number
K171172 000
K182438 000