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Diva

FDA UDI

Class I (US FDA UDI)

by Diva International Inc

Identity

Trade Name
Diva FDA UDI
Generic Name
Menstrual underwear FDA UDI
Device Name
Diva Period Underwear - BL (Each) - Bikini Black XL-XXL FDA UDI
Model / Reference
XL-XXL FDA UDI
Description
Diva Period Underwear - BL (Each) - Bikini Black XL-XXL FDA UDI

Identifiers

Catalog Number
FGUN060201BK03 FDA UDI
Primary DI / UDI-DI
00841445000480 FDA UDI
FDA Product Code
NUQ FDA UDI
GMDN Term
Menstrual underwear FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
884.5435 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Menstrual underwear

Diva by Diva International Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Menstrual underwear.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI acec8adc-933a-462e-97c1-a854bf086e83 35 fields · synced May 30, 2026