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Saalt Menstrual Cup

FDA UDI

Class II (US FDA UDI)

by Saalt, LLC

Identity

Trade Name
Saalt Menstrual Cup FDA UDI
Generic Name
Menstrual cup/disc, non-latex, reusable FDA UDI
Device Name
Saalt Cup Small Purple FDA UDI
Model / Reference
SC0014R FDA UDI
Description
Saalt Cup Small Purple FDA UDI

Identifiers

Primary DI / UDI-DI
00810050720762 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

No

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

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

Saalt Menstrual Cup by Saalt, 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
Saalt, LLC

Sources (1)

  • FDA UDI c6ee2b07-d45c-4ca0-8e12-b8725e4e54a8 33 fields · synced May 30, 2026