GUDIDData
gudid Primary ID: HyBase V6

Mindray (UDI HyBase V6)

Manufactured by Nanjing Mindray Bio-Medical Electronics Co.,Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Mindray - Primary ID HyBase V6

Device Regulatory Overview

The Mindray (Model/Catalog Number: HyBase V6) is a medical device manufactured by Nanjing Mindray Bio-Medical Electronics Co.,Ltd. This product is indexed under FDA Product Code / Category Classification FQO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
HyBase V6
Product Code / EMDN
FQO
Device Name
Database Sync Date
2026-08-09 09:05:26

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 Mindray?

The registered manufacturer of record for Mindray is Nanjing Mindray Bio-Medical Electronics Co.,Ltd.

What is the Primary UDI-DI identifier for Mindray?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is HyBase V6.

What classification code is assigned to this device?

This device is registered under product classification code FQO.

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