GUDIDData
eudamed_udi Primary ID: 00884838082588

IntelliVue X3 (UDI 00884838082588)

Manufactured by Philips Medizin Systeme Böblingen GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for IntelliVue X3 - Primary ID 00884838082588

Device Regulatory Overview

The IntelliVue X3 (Model/Catalog Number: 867030) is a medical device manufactured by Philips Medizin Systeme Böblingen GmbH. This product is indexed under FDA Product Code / Category Classification Z1203020299 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
867030
Product Code / EMDN
Z1203020299
Device Name
X3/MX100
Database Sync Date
2026-08-09 16:28:50

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 IntelliVue X3?

The registered manufacturer of record for IntelliVue X3 is Philips Medizin Systeme Böblingen GmbH.

What is the Primary UDI-DI identifier for IntelliVue X3?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00884838082588.

What classification code is assigned to this device?

This device is registered under product classification code Z1203020299.

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