FDA UDI In Commercial Distribution 🇺🇸 United States

SKYN

DI: 00070907001134 · Model: 0113 · SURETEX LIMITED - BRANCH
Product Codes
2
GMDN Terms
2
Identifiers
4
Pkg Device Count
13

Basic Information

Brand Name
SKYN
Primary DI
00070907001134
Version / Model
0113
Company Name
SURETEX LIMITED - BRANCH
Labeler DUNS
672044515
Distribution Status
In Commercial Distribution
Device Count in Pkg
13
Record Status
Published
Publish Date
2023-06-27
Public Version
1
Public Version Date
2023-07-05
Public Version Status
New
Public Device Record Key
6ee1c327-e793-4806-a7ae-2ad606fa5562

Device Description

SKYN ORIGINAL 24CT + 1 NATURALLY ENDLESS SACHET

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
NUC Lubricant, Personal

GMDN Terms

Code Name
34151 Basic male condom, synthetic polymer
60412 Sexual lubricant

Identifiers

Type ID
Unit of Use 80070907102165
Primary 00070907001134
Package 10070907001131
Package 30070907001135

Customer Contacts

Phone
848-229-3224

Premarket Submissions

Submission Number Supplement Number
K171172 000
K221243 000