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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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CC-100 HW6.0 Series — 4 UDI-DI variants, MDR (Visia imaging SRL)

MD Atlas
Visia imaging SRL

Data from EUDAMED, last updated May 30, 2026

CC-100 HW6.0 Series

803402877VISUALCHART1L6

4 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: Visia imaging SRL

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 803402877VISUALCHART1L6
Device name: CC-100 HW6.0 Series
Device model: CC-100 HW6.0 / CC-100XP HW6.0
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 14, 2022

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

4 UDI-DI variants

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Applied filters

basicUdiUlid01FZAZEARR5N3M19NYQNDBYDXB

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

42-000008708034028770319
42-000286608034028770555
42-000008808034028770326
42-000286708034028770579