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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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IGT-Tubes Family — 10 UDI-DI variants, MDR

MD Atlas
Philips Medical Systems DMC GmbH

Data from EUDAMED, last updated May 23, 2026

IGT-Tubes Family

0884838BM496TM

10 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: 0884838BM496TM
Device name: IGT-Tubes Family
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jan 16, 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

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HM8KH35SX10WYJ5ZZVZAGWYP

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

MRC 200 0407 ROT-GS 100400884838076181
MRC 200 0407 ROT-GS 100400884838092945
MRC 200 0407 ROT-GS 1004 PREOWNED00884838076044
MRC 200 0508 ROT-GS 100300884838076204
MRC 200 0508 ROT-GS 100300884838092952
MRC 200 0508 ROT-GS 1003 PREOWNED00884838076020
MRC 200 0508 ROT-GS 100500884838076334
MRC 200+ 0407 ROT-GS 100400884838092976
MRC 200+ 0407 ROT-GS 100800884838092921
MRC 200+ 0508 ROT-GS 100300884838092969