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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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soluzione oftalmica — 11 UDI-DI variants, MDR (IROMED GROUP S.R.L.)

MD Atlas
IROMED GROUP S.R.L.

Data from EUDAMED, last updated May 31, 2026

soluzione oftalmica

805701817DTHED8

11 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: IROMED GROUP S.R.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805701817DTHED8
Device name: soluzione oftalmica
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Apr 16, 2026

Manufacturer & authorised representative

Manufacturer

Name: IROMED GROUP S.R.L.
SRN: IT-MF-000031267
Country: Italy
Email: regulatoryaffairs@iromedgroup.com
Phone: +39 06 92595490

Variants by status

UDI-DI variants

11 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KPBAFJ1WZ9KJZ8RP6PWESEKW

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

DTHE009V08057018171231
DTHE005V08057018171200
DTHE007V08057018171217
DTHE001V08057018170043
DTHE001S08057018170524
DTHE002V08057018171194
DTHE003V08057018170180
DTHE004V08057018170470
DTHE004S08057018170999
DTHE006S08057018170555
DTHE006V08057018170128