FDA UDI In Commercial Distribution 🇺🇸 United States

Tampax

DI: 00073010380103 · Model: Tampax · PROCTER & GAMBLE MANUFACTURING COMPANY, THE
Product Codes
1
GMDN Terms
1
Identifiers
5
Pkg Device Count
20

Basic Information

Brand Name
Tampax
Primary DI
00073010380103
Version / Model
Tampax
Company Name
PROCTER & GAMBLE MANUFACTURING COMPANY, THE
Labeler DUNS
004238200
Distribution Status
In Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2016-09-15
Public Version
3
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
1a8d9708-0820-466d-bea5-132b247baf2c

Device Description

TAMPAX OEF SUPER 20CT

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
HEB TAMPON, MENSTRUAL, UNSCENTED

GMDN Terms

Code Name
35694 Menstrual tampon, unscented

Identifiers

Type ID
Primary 00073010380103
Package 20073010380107
Package 00073010380127
Package 00001490601463
Unit of Use 50073010380108