eudamed_udi Primary ID: 06955797762126

Trocar kit (UDI 06955797762126)

Manufactured by Unimicro Medical Systems (Shenzhen) Co., Ltd

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Trocar kit (Model/Catalog Number: UNTR-CII1) is a medical device manufactured by Unimicro Medical Systems (Shenzhen) Co., Ltd. This product is indexed under FDA Product Code / Category Classification K01010103 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: UNTR-CII1
Product Code / EMDN: K01010103
Device Name: Visible Trocar Set
Database Sync Date: 2026-08-09 16:45:07

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 Trocar kit?

The registered manufacturer of record for Trocar kit is Unimicro Medical Systems (Shenzhen) Co., Ltd.

What is the Primary UDI-DI identifier for Trocar kit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06955797762126.

What classification code is assigned to this device?

This device is registered under product classification code K01010103.

Similar Classification Devices (K01010103)

Other Devices by Unimicro Medical Systems (Shenzhen) Co., Ltd

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