Skip to content

Devices Categories Manufacturers Importers Certifiers Authorities Reps. Representatives

Results for “Tampax Radiant”

Name, manufacturer or identifier

Manufacturer (optional)

Filters

Registry EUDAMED FDA 510(k) FDA PMA GUDID 117

Country / market United States 117

Risk class Class I Class IIa Class IIb Class III Class II (US) 117

More classes (11)

Class A Class B Class C Class D IVD General IVD Annex II List A IVD Annex II List B IVD for self-testing Active implantable (AIMDD) Unclassified (FDA) Not classified (FDA)

Verified Validated only

Category (EMDN)

Browse by category

117 devices foundsorted by relevance

Device · Manufacturer · Authorizations

Tampax Radiant, Tampax Pocket Pearl UDI-DI 40073010024586

Procter & Gamble Manufacturing Company, The,FDA registration: United States Class II

None GUDID II
9 variants
- Tampax Radiant, Tampax Pocket Pearl UDI-DI 40037000958923
- Tampax Radiant, Tampax Pocket Pearl UDI-DI 40073010023633
- Tampax Radiant, Tampax Pocket Pearl UDI-DI 40073010024524
- See all variants of this device
Tampax Radiant UDI-DI 10073010713069

Procter & Gamble Manufacturing Company, The,FDA registration: United States Class II

None GUDID II
84 variants
- Tampax Radiant UDI-DI 00073010015371
- Tampax Radiant UDI-DI 00073010710429 Withdrawn
- Tampax Radiant UDI-DI 00073010711570
- Tampax Radiant UDI-DI 10073010716381
- Tampax Radiant UDI-DI 10073010719061
- Tampax Radiant UDI-DI 20073010715114
- Tampax Radiant UDI-DI 40073010022551
- Tampax Radiant UDI-DI 40073010023466
- Tampax Radiant UDI-DI 40073010024463
- Tampax Radiant UDI-DI 40073010713084
- Tampax Radiant UDI-DI 40073010716283
- Tampax Radiant UDI-DI 40073010716399
- See all variants of this device
Tampax Pearl, Tampax Radiant UDI-DI 40073010024531

Procter & Gamble Manufacturing Company, The,FDA registration: United States Class II

None GUDID II
18 variants
- Tampax Pearl, Tampax Radiant UDI-DI 40037000141714
- See all variants of this device
Tampax Radiant, Tampax Pocket Radiant UDI-DI 40073010718751

Procter & Gamble Manufacturing Company, The,FDA registration: United States Class II

None GUDID II
2 variants
- See all variants of this device

Showing 41-60 of 117

deviCERTS Global Medical Device Regulatory Database

About [email protected]

© 2026 deviCERTS — digitaly.site