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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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ImgView — 1 UDI-DI variant, MDR (RAR s.r.l.)

MD Atlas
RAR s.r.l.

Data from EUDAMED, last updated May 31, 2026

ImgView

805759209IMGVIEWXU

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: RAR s.r.l.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805759209IMGVIEWXU
Device name: ImgView
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Special device type: refdata.special-mdr-device-type.software
Version date: Apr 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: RAR s.r.l.
SRN: IT-MF-000030103
Country: Italy
Email: info@rartech.it
Phone: +39 045 4730768

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KQCJYGGPR8AJ83R541DD652Z

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

ImgView08057592090010