Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

X-ray tubes — 77 UDI-DI variants, MDR

MD Atlas
I.A.E. INDUSTRIA APPLICAZIONI ELETTRONICHE S.P.A.

Data from EUDAMED, last updated May 30, 2026

X-ray tubes

805930749385G4

77 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: I.A.E. INDUSTRIA APPLICAZIONI ELETTRONICHE S.P.A.

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805930749385G4
Device name: X-ray tubes
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 12, 2023

Manufacturer & authorised representative

Manufacturer

Name: I.A.E. INDUSTRIA APPLICAZIONI ELETTRONICHE S.P.A.
SRN: IT-MF-000021626
Country: Italy
Email: iaexray@iae.it
Phone: +39 02 66303255

Variants by status

UDI-DI variants

77 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01H07X8GJ2W72BXE84264XNGSY

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

RTM 72 HS08059307490399
RTM 75 H08059307490412
RTM 75 HS08059307491518
RTM 77 H08059307491570
RTM 77 H08059307490443
RTM 77 H08059307490436
RTM 77 HS 0.6/1.2508059307491563
RTM 78 H08059307490450
RTM 78 HS08059307490481
RTM 78 HS08059307491495
RTM 780 H08059307490511
RTM 780 HS 0.3/0.608059307491594
RTM 782 H08059307490528
RTM 782 H08059307490535
RTM 782 HS08059307491556
RTM 782 HS08059307490559
RTM 80 H08059307491525
RTM 80 H08059307491549
RTM 80 HS08059307490580
RTM 80 HS08059307491532
RTM 90 H08059307490610
RTM 90 H08059307490627
RTM 90 H08059307490597
RTM 90 HS08059307490696
RTM 90 HS08059307490702

1 2 3 4