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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-ray viewers — 6 UDI-DI variants, MDR (Titanox S.r.l.)

MD Atlas
Titanox S.r.l.

Data from EUDAMED, last updated May 31, 2026

X-ray viewers

805930470M05H4

6 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: Titanox S.r.l.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805930470M05H4
Device name: X-ray viewers
Device model: X-ray viewers
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: Titanox S.r.l.
SRN: IT-MF-000020325
Country: Italy
Email: info@titanox.it
Phone: +390375394065

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSJBW7JDTJCSKXHJCZSFND0A

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

M60404308059304703546
M608043/GM08059304703577
M604043/M08059304703553
M61204308059304703584
M60804308059304703560
M612043/GM08059304703591