eudamed_udi Primary ID: 26970614965621

Hydrogen Peroxide Cartridge (UDI 26970614965621)

Manufactured by Shinva Medical Instrument Co., Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Hydrogen Peroxide Cartridge (Model/Catalog Number: HC1001-E) is a medical device manufactured by Shinva Medical Instrument Co., Ltd.. This product is indexed under FDA Product Code / Category Classification S900101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: HC1001-E
Product Code / EMDN: S900101
Device Name: Hydrogen Peroxide Cartridge
Database Sync Date: 2026-08-09 16:30:18

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 Hydrogen Peroxide Cartridge?

The registered manufacturer of record for Hydrogen Peroxide Cartridge is Shinva Medical Instrument Co., Ltd..

What is the Primary UDI-DI identifier for Hydrogen Peroxide Cartridge?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 26970614965621.

What classification code is assigned to this device?

This device is registered under product classification code S900101.

Similar Classification Devices (S900101)

Other Devices by Shinva Medical Instrument Co., Ltd.

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