FDA UDI In Commercial Distribution 🇺🇸 United States

Tampax

DI: 00073010715301 · Model: Tampax Cup · PROCTER & GAMBLE MANUFACTURING COMPANY, THE
Product Codes
1
GMDN Terms
1
Identifiers
6
Pkg Device Count
1

Basic Information

Brand Name
Tampax
Primary DI
00073010715301
Version / Model
Tampax Cup
Company Name
PROCTER & GAMBLE MANUFACTURING COMPANY, THE
Labeler DUNS
004238200
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-08-30
Public Version
1
Public Version Date
2021-09-07
Public Version Status
New
Public Device Record Key
1c0c3418-6c06-4b57-827d-b77b5f3b6da0

Device Description

Tampax Cup Regular Flow

Device Characteristics

Single Use
No
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
HHE Cup, menstrual

GMDN Terms

Code Name
47728 Menstrual cup, non-latex, reusable

Identifiers

Type ID
Package 10073010715360
Primary 00073010715301
Package 10073010715308
Package 20073010715305
Package 40073010715309
Package 40073010715361