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Kind Cup

FDA UDI

Class II (US FDA UDI)

by Wevotopia LLC

Identity

Trade Name
Kind Cup FDA UDI
Generic Name
Menstrual cup/disc, non-latex, reusable FDA UDI
Device Name
Duo Pack Aqua of one size small and one size regular menstrual cups with aqua pigment. FDA UDI
Model / Reference
Duo Aqua FDA UDI
Description
Duo Pack Aqua of one size small and one size regular menstrual cups with aqua pigment. FDA UDI

Identifiers

Catalog Number
DA FDA UDI
Primary DI / UDI-DI
G357DA0 FDA UDI
FDA Product Code
HHE FDA UDI
GMDN Term
Menstrual cup/disc, non-latex, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.5400 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Menstrual cup/disc, non-latex, reusable

Kind Cup by Wevotopia LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Menstrual cup/disc, non-latex, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Wevotopia LLC

Sources (1)

  • FDA UDI 7200cdcf-afc1-446b-b29c-9ebe5f46651d 34 fields · synced Jun 1, 2026