FDA UDI In Commercial Distribution 🇺🇸 United States

Kotex

DI: 07702425810501 · Model: Pad · KIMBERLY CLARK COLOMBIA HOLDING LTDA
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
10

Basic Information

Brand Name
Kotex
Primary DI
07702425810501
Version / Model
Pad
Company Name
KIMBERLY CLARK COLOMBIA HOLDING LTDA
Labeler DUNS
881043603
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2021-12-15
Public Version
1
Public Version Date
2021-12-23
Public Version Status
New
Public Device Record Key
bc0f1a64-9452-4d4d-abde-fe7d9d0790bc

Device Description

TOA FEM KOT PURE UF TELA C/A 12X10

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 17702425810508
Primary 07702425810501
Unit of Use 07441008100249

Customer Contacts