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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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EYE BATH — 2 UDI-DI variants, MDR (DIATECH SRL)

MD Atlas
DIATECH SRL

Data from EUDAMED, last updated May 31, 2026

EYE BATH

8055162105EYEBATHD3

2 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: DIATECH SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8055162105EYEBATHD3
Device name: EYE BATH
Device model: EYE BATH
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 18, 2025

Manufacturer & authorised representative

Manufacturer

Name: DIATECH SRL
SRN: IT-MF-000029128
Country: Italy
Email: francesco.ronchi@diatechsrl.it
Phone: +390314978519

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JMC7C2X67FCWM1VP8A6C7J3K

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

EYE BATH80551621050036
ICA EYE BATH80551621050135