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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
18 Organic Cotton Regular Tampons FDA UDI
Model / Reference
FG-TMP-REF00001800 FDA UDI
Description
18 Organic Cotton Regular Tampons FDA UDI

Identifiers

Primary DI / UDI-DI
05060994741056 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
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

No

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

Category: Menstrual tampon, unscented

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

Similar devices

Also classified as Menstrual tampon, unscented.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6af1b68f-6e02-4f80-bced-1488071a870c 34 fields · synced Jun 8, 2026