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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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MYAH — 2 UDI-DI variants, MDR (Visia imaging SRL)

MD Atlas
Visia imaging SRL

Data from EUDAMED, last updated May 30, 2026

MYAH

803402877BIOMETER2C7

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Visia imaging SRL

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 803402877BIOMETER2C7
Device name: MYAH
Device model: MYAH; MYOPIA EXPERT 700
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Nov 5, 2024

Manufacturer & authorised representative

Manufacturer

Name: Visia imaging SRL
SRN: IT-MF-000015628
Country: Italy
Email: quality.hcs.it@topcon.com
Phone: +39 055 9121635

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HXENET8NCXKCXY6A1V31PYWQ

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

42-000098308034028770340
BMT1IV08034028770395