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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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Philips CT Big Bore System — 2 UDI-DI variants, MDR

MD Atlas
Philips Medical Systems Nederland B.V.

Data from EUDAMED, last updated May 30, 2026

Philips CT Big Bore System

0884838BM277T7

2 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 Nederland B.V.

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 0884838BM277T7
Device name: Philips CT Big Bore System
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Dec 2, 2024

Manufacturer & authorised representative

Manufacturer

Name: Philips Medical Systems Nederland B.V.
SRN: NL-MF-000001489
Country: Netherlands
Email: eudamed@philips.com
Phone: n/a

Variants by status

UDI-DI variants

2 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JE4C7ND926H6BM7JS7DM8QZ1

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

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