FDA UDI In Commercial Distribution 🇺🇸 United States

SKYN

DI: 00070907271032 · Model: 7103 · SURETEX LIMITED - BRANCH
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
3

Basic Information

Brand Name
SKYN
Primary DI
00070907271032
Version / Model
7103
Company Name
SURETEX LIMITED - BRANCH
Labeler DUNS
672044515
Distribution Status
In Commercial Distribution
Device Count in Pkg
3
Record Status
Published
Publish Date
2016-07-11
Public Version
8
Public Version Date
2023-07-27
Public Version Status
Update
Public Device Record Key
7a44c7da-7e0f-4e3d-b1ac-1bdd52f550a7

Device Description

SKYN SELECTION 3CT (ORIGINAL, EXTRA STUDDED, ELITE EXTRA LUBE)

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
Primary 00070907271032
Unit of Use 80070907140570
Package 10070907271039
Package 30070907271033

Premarket Submissions

Submission Number Supplement Number
K171172 000