Kotex

Basic Information

• Brand Name: Kotex
• Primary DI: 07702425810853
• Version / Model: Liner
• Company Name: KIMBERLY CLARK COLOMBIA HOLDING LTDA
• Labeler DUNS: 881043603
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 120
• 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: fc8161f0-280a-4bb0-8b1f-b23214e79631

Device Description

PRO DIA KOT PURE REG 12X120

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	Medical Specialty	Regulation #	Device Class
NRC	Pads, menstrual, scented-deodorized	Obstetrics/Gynecology	884.5425	1

GMDN Terms

Code	Name	Definition	Implantable	Status
40545	Menstrual pad, unscented	A non-deodorized, feminine hygiene product (a pad) that is held in place externally to absorb menstrual or other vaginal discharge. This is a single-use device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Package	17702425810850	GS1	Case	12	In Commercial Distribution
Primary	07702425810853	GS1
Unit of Use	07441008100232	GS1

Customer Contacts

• Phone: [phone]
• Email: [email protected]