← Back to catalogue

Amazon Basics

FDA UDI

Class II (US FDA UDI)

by Amazon.com Services, LLC

Identity

Trade Name
Amazon Basics FDA UDI
Generic Name
Menstrual cup/disc, non-latex, reusable FDA UDI
Device Name
Amazon Basics Menstrual Cup FDA UDI
Model / Reference
B098VHYX2M FDA UDI
Description
Amazon Basics Menstrual Cup FDA UDI

Identifiers

Catalog Number
B098VHYX2M FDA UDI
Primary DI / UDI-DI
00195515017947 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
Not 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Amazon Basics by Amazon.com Services, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 6289e5b8-0c25-41c8-bb62-7f047589d50f 36 fields · synced May 30, 2026