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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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X-Tray — 5 UDI-DI variants, MDR (Krucom AB)

MD Atlas
Krucom AB

Data from EUDAMED, last updated May 31, 2026

X-Tray

7333531_KRUCOM_X-TRAY_QY

5 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: Krucom AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 7333531_KRUCOM_X-TRAY_QY
Device name: —
Device model: X-Tray
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Special device type: refdata.special-mdr-device-type.software
Version date: May 27, 2025

Manufacturer & authorised representative

Manufacturer

Name: Krucom AB
SRN: SE-MF-000047914
Country: Sweden
Email: office@krucom.com

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01JW88WFP4M39QR9WXYP6M4XBT

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

3.20.007333531000014
3.22.107333531000045
3.23.007333531000052
3.24.007333531000069
3.25.007333531000076