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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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TOPOGRAFO CORNEALE — 3 UDI-DI variants, MDR (SBM SISTEMI S.R.L.)

MD Atlas
SBM SISTEMI S.R.L.

Data from EUDAMED, last updated May 31, 2026

TOPOGRAFO CORNEALE

805614988OS1000D4

3 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: SBM SISTEMI S.R.L.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805614988OS1000D4
Device name: TOPOGRAFO CORNEALE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: SBM SISTEMI S.R.L.
SRN: IT-MF-000026683
Country: Italy
Email: amministrazione@sbmsistemi.com
Phone: +39 011 19923378

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KPQMX49E2GRTYY1KJVXX8K2D

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

15018E08056149880180
1501808056149880111
15018T08056149880234