FDA UDI Not in Commercial Distribution 🇺🇸 United States

U By Kotex

DI: 00036000534719 · Model: Pad · KIMBERLY-CLARK GLOBAL SALES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
14

Basic Information

Brand Name
U By Kotex
Primary DI
00036000534719
Version / Model
Pad
Company Name
KIMBERLY-CLARK GLOBAL SALES, INC.
Labeler DUNS
829568273
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
14
Record Status
Published
Publish Date
2020-08-06
Public Version
3
Public Version Date
2022-09-30
Public Version Status
Update
Public Device Record Key
05315af5-1dc0-4a6a-b9b0-dcfc60320d0b
Distribution End Date
2022-09-30

Device Description

U BY KOTEX SUPRPREM ULTRATHN HVYWNG PAD 14

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HHD Pad, menstrual, unscented

GMDN Terms

Code Name
40545 Menstrual pad, unscented

Identifiers

Type ID
Package 10036000534716
Primary 00036000534719
Unit of Use 00036000536768

Customer Contacts