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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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Fixed equipment for radioscopy and… — 2 UDI-DI variants, MDR

MD Atlas
Technix S.p.A.

Data from EUDAMED, last updated May 30, 2026

Fixed equipment for radioscopy and radiography

805330759ARCHIACFJ

2 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: Technix S.p.A.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805330759ARCHIACFJ
Device name: Fixed equipment for radioscopy and radiography
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jun 7, 2022

Manufacturer & authorised representative

Manufacturer

Name: Technix S.p.A.
SRN: IT-MF-000007797
Country: Italy
Email: info@technix.it
Phone: +390353846611

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01G4ZBVSWCZA0M4HDDRP3VAR5P

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

NAUTILUS08053307590189
QUANTIC08053307590172