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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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DigiTrakXTPatientCable Short/Medium/Long — 3 UDI-DI variants, MDR

MD Atlas
Philips Medizin Systeme Böblingen GmbH

Data from EUDAMED, last updated May 23, 2026

DigiTrakXTPatientCable Short/Medium/Long

0884838BM1862N7

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Philips Medizin Systeme Böblingen GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0884838BM1862N7
Device name: DigiTrakXTPatientCable Short/Medium/Long
Device model: DigiTrakXTPatientCable Short/Medium/Long
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 21, 2025

Manufacturer & authorised representative

Manufacturer

Name: Philips Medizin Systeme Böblingen GmbH
SRN: DE-MF-000006026
Country: Germany
Email: eudamed@philips.com
Phone: n/a

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01K379X55PETSTZ4MK68XDF9ZB

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

DigiTrak XT Patient Cable Long00884838117457
DigiTrak XT Patient Cable Medium00884838117440
DigiTrak XT Patient Cable Short00884838117433