FDA UDI In Commercial Distribution 🇺🇸 United States

Tampax

DI: 00073010720084 · Model: Tampax Pearl · PROCTER & GAMBLE MANUFACTURING COMPANY, THE
Product Codes
1
GMDN Terms
1
Identifiers
5
Pkg Device Count
30

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Basic Information

Brand Name
Tampax
Primary DI
00073010720084
Version / Model
Tampax Pearl
Company Name
PROCTER & GAMBLE MANUFACTURING COMPANY, THE
Labeler DUNS
004238200
Distribution Status
In Commercial Distribution
Device Count in Pkg
30
Record Status
Published
Publish Date
2025-04-29
Public Version
2
Public Version Date
2025-12-18
Public Version Status
Update
Public Device Record Key
aad9e022-0a8a-4a6d-82cb-b4fc6eea8dbe

Device Description

Tampax Compact Pearl Duo - Super, Super Plus

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
No
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 40073010720082
Package 10073010720081
Package 20073010720088
Primary 00073010720084
Unit of Use 50073010720089