GUDIDData
gudid Primary ID: XMR0001

Mindray (UDI XMR0001)

Manufactured by GaleMed Xiamen Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Mindray - Primary ID XMR0001

Device Regulatory Overview

The Mindray (Model/Catalog Number: XMR0001) is a medical device manufactured by GaleMed Xiamen Co., Ltd.. This product is indexed under FDA Product Code / Category Classification BZO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
XMR0001
Product Code / EMDN
BZO
Device Name
Gas Sampling Line, Adult 2.5 m
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
}
                            

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Mindray?

The registered manufacturer of record for Mindray is GaleMed Xiamen Co., Ltd..

What is the Primary UDI-DI identifier for Mindray?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is XMR0001.

What classification code is assigned to this device?

This device is registered under product classification code BZO.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint