Tampax

Basic Information

• Brand Name: Tampax
• Primary DI: 00073010714533
• Version / Model: Tampax Pearl
• Company Name: PROCTER & GAMBLE MANUFACTURING COMPANY, THE
• Labeler DUNS: 004238200
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 32
• Record Status: Published
• Publish Date: 2019-12-13
• Public Version: 2
• Public Version Date: 2022-06-10
• Public Version Status: Update
• Public Device Record Key: 424a6bfe-53c6-4172-954a-d616e01d20b1

Device Description

Tampax Pearl Ultra

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: No
• 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
HEB	Tampon, menstrual, unscented	Obstetrics/Gynecology	884.5470	2

GMDN Terms

Code	Name	Definition	Implantable	Status
35694	Menstrual tampon, unscented	A non-deodorized plug made of cellulosic or synthetic material that is inserted into the vagina to absorb menstrual blood 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	20073010714537	GS1	inner pack	3	In Commercial Distribution
Primary	00073010714533	GS1
Package	40073010714531	GS1	pallet	27	In Commercial Distribution
Package	10073010714530	GS1	case	4	In Commercial Distribution
Unit of Use	50073010714538	GS1