GUDIDData
eudamed_udi Primary ID: 06943831410430

Unspecified Brand (UDI 06943831410430)

Manufactured by Hangzhou Mindray Medical Technology Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 06943831410430

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: 221-01785) is a medical device manufactured by Hangzhou Mindray Medical Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification L031202 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
221-01785
Product Code / EMDN
L031202
Device Name
Reducer Sleeve
Database Sync Date
2026-08-09 16:45:59

Full Regulatory Attributes

🔒 Token Gated
{
    "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 Unspecified Brand?

The registered manufacturer of record for Unspecified Brand is Hangzhou Mindray Medical Technology Co., Ltd..

What is the Primary UDI-DI identifier for Unspecified Brand?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06943831410430.

What classification code is assigned to this device?

This device is registered under product classification code L031202.

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