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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

ERE5C05414904015490
5VCEO05414904128336
51BN805414904175682
51BPD05414904175705
51BL405414904175668
51BOB05414904175699
51BM605414904175675
51BSK05414904175736
51BRH05414904175729
51BQF05414904175712
ERRU605414904014073
ERRT405414904014080
ERRWB05414904014059
ERRV805414904014066
EZ5L505414904011959
EZ5J105414904011973
EZ5K305414904011966

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