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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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DR 400 5520 — 3 UDI-DI variants, MDR (Agfa NV)

MD Atlas
Agfa NV

Data from EUDAMED, last updated May 23, 2026

DR 400 5520

5414904272848YZ

3 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: Agfa NV

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 5414904272848YZ
Device name: DR 400 5520
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Aug 22, 2024

Manufacturer & authorised representative

Manufacturer

Name: Agfa NV
SRN: BE-MF-000000571
Country: Belgium
Email: agfamedimg@gmail.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J5X3SW36AZNH5G80RSP4PS88

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

58UCJ05414904217870
51FS105414904176252
MBFTK05414904281321