eudamed_udi Primary ID: 06975575100056

Menstrual Cup (UDI 06975575100056)

Manufactured by Xi'an Furuize Biotechnology Co., Ltd.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Menstrual Cup (Model/Catalog Number: REF-005) is a medical device manufactured by Xi'an Furuize Biotechnology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification A0699 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: REF-005
Product Code / EMDN: A0699
Device Name: Menstrual Cup
Database Sync Date: 2026-08-09 16:59:42

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of Menstrual Cup?

The registered manufacturer of record for Menstrual Cup is Xi'an Furuize Biotechnology Co., Ltd..

What is the Primary UDI-DI identifier for Menstrual Cup?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975575100056.

What classification code is assigned to this device?

This device is registered under product classification code A0699.

Similar Classification Devices (A0699)

Other Devices by Xi'an Furuize Biotechnology Co., Ltd.

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