Besmed Menstrual Cup

FDA UDI

Class II (US FDA UDI)

by Besmed Health Business Corp.

Identity

Trade Name: Besmed Menstrual Cup FDA UDI
Generic Name: Menstrual cup/disc, non-latex, reusable FDA UDI
Device Name: Small White Menstrual Cup FDA UDI
Model / Reference: PE-34146 FDA UDI
Description: Small White Menstrual Cup FDA UDI

Identifiers

Primary DI / UDI-DI: 04716770341460 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Microwave Radiation FDA UDI

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

Besmed Menstrual Cup by Besmed Health Business Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Besmed Health Business Corp.

Sources (1)

FDA UDI 140e9311-5cb1-4ed0-8c3b-6d96411fced2 33 fields · synced May 30, 2026