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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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CT Tubes Family — 13 UDI-DI variants, MDR

MD Atlas
Philips Medical Systems DMC GmbH

Data from EUDAMED, last updated May 23, 2026

CT Tubes Family

0884838BM494TH

13 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Philips Medical Systems DMC GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 0884838BM494TH
Device name: CT Tubes Family
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Aug 30, 2024

Manufacturer & authorised representative

Manufacturer

Name: Philips Medical Systems DMC GmbH
SRN: DE-MF-000005362
Country: Germany
Email: eudamed@philips.com
Phone: n/a

Variants by status

UDI-DI variants

13 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J6H2Q7EPGSS7BG7074F3N6CT

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

CT300000884838121379
CT400000884838105454
CT400000884838105430
CT400000884838121386
PHILIPS MRC 60000884838076310
PHILIPS MRC 600 CPO00884838093003
PHILIPS MRC 80000884838076327
PHILIPS MRC 800 CPO00884838093010
PHILIPS MRC 88000884838076396
PHILIPS MRC 880 CPO00884838093522
vMRC Performance00884838120501
vMRC Performance00884838107168
vMRC Performance00884838085589