GUDIDData
gudid Primary ID: 6200-30-09688

TUBE,NIBP,ADU/PED/INF,CONN,3M (UDI 6200-30-09688)

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

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TUBE,NIBP,ADU/PED/INF,CONN,3M - Primary ID 6200-30-09688

Device Regulatory Overview

The TUBE,NIBP,ADU/PED/INF,CONN,3M (Model/Catalog Number: 6200-30-09688) is a medical device manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. This product is indexed under FDA Product Code / Category Classification MWI within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
6200-30-09688
Product Code / EMDN
MWI
Device Name
Database Sync Date
2026-08-09 09:11:05

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 TUBE,NIBP,ADU/PED/INF,CONN,3M?

The registered manufacturer of record for TUBE,NIBP,ADU/PED/INF,CONN,3M is Shenzhen Mindray Bio-Medical Electronics Co., Ltd..

What is the Primary UDI-DI identifier for TUBE,NIBP,ADU/PED/INF,CONN,3M?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6200-30-09688.

What classification code is assigned to this device?

This device is registered under product classification code MWI.

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