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Daye

FDA UDI

Class II (US FDA UDI)

by Tampon Innovations Ltd Ood

Identity

Trade Name
Daye FDA UDI
Generic Name
Menstrual tampon, unscented FDA UDI
Device Name
Retail Tampon box - 9 coated regular tampons + 9 organic regular tampons FDA UDI
Model / Reference
FG-TMP-RET09000900 FDA UDI
Description
Retail Tampon box - 9 coated regular tampons + 9 organic regular tampons FDA UDI

Identifiers

Primary DI / UDI-DI
05060994740592 FDA UDI
510(k) Number
K223883 FDA UDI
FDA Product Code
HEB FDA UDI
GMDN Term
Menstrual tampon, unscented FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.5470 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Daye by Tampon Innovations Ltd Ood — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K223883 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tampon Innovations Ltd Ood

Sources (1)

  • FDA UDI aeb04110-b745-463c-960a-5e025774a7b4 35 fields · synced May 30, 2026