FDA UDI In Commercial Distribution 🇺🇸 United States

Tampax

DI: 00073010021433 · Model: Tampax Radiant · PROCTER & GAMBLE MANUFACTURING COMPANY, THE
Product Codes
1
GMDN Terms
1
Identifiers
6
Pkg Device Count
32

Basic Information

Brand Name
Tampax
Primary DI
00073010021433
Version / Model
Tampax Radiant
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
2016-09-15
Public Version
3
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
6a59885f-a1aa-4f79-9c50-4e34f022613c

Device Description

TAMPAX RADIANT REGULAR 32CT

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
Package 40073010021431
Package 10073010021430
Primary 00073010021433
Package 40073010021936
Package 00073010021938
Unit of Use 50073010021438