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Sustain Natural Menstrual Cup

FDA UDI

Class II (US FDA UDI)

by Claripharm

Identity

Trade Name
SUSTAIN NATURAL MENSTRUAL CUP FDA UDI
Generic Name
Menstrual cup/disc, non-latex, reusable FDA UDI
Device Name
MENSTRUAL CUP FDA UDI
Model / Reference
SIZE 1 FDA UDI
Description
MENSTRUAL CUP FDA UDI

Identifiers

Catalog Number
403CUPS1 FDA UDI
Primary DI / UDI-DI
37012713000486 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

Yes

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 cup/disc, non-latex, reusable

Sustain Natural Menstrual Cup by Claripharm — 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
Claripharm

Sources (1)

  • FDA UDI 4e3aa26e-1d8c-4c45-b08d-0e9d2d5c4b90 35 fields · synced Jun 1, 2026