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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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Hard Copy Film — 42 UDI-DI variants, MDR (Agfa NV)

MD Atlas
Agfa NV

Data from EUDAMED, last updated May 23, 2026

Hard Copy Film

5414904273005XE

42 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: Agfa NV

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5414904273005XE
Device name: Hard Copy Film
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 27, 2025

Manufacturer & authorised representative

Manufacturer

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

Variants by status

UDI-DI variants

42 UDI-DI variants

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Applied filters

basicUdiUlid01JN3TK0YF8Y4KGYAPWCHYRR38

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

54R6V05414904194690
54R5T05414904194683
54R8Z05414904195710
54R7X05414904195703
XCMX305414904236376
59CM805414904220535
5YHZ705414904161869
5YH2C05414904161883
5YH3E05414904161890
5YH1A05414904161876
5YH5J05414904161845
5YH6L05414904161852
5YH4G05414904161838
51BDP05414904175194
51BGV05414904175620
51BCN05414904175187
51BHX05414904175637
51BJZ05414904175644
EKL9M05414904025765
EKL3805414904025574
EKL4B05414904025581
EKL7H05414904025611
5VCDM05414904128367
ERE7G05414904015476
ERE6E05414904015483

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