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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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SCHWIND AMARIS — 3 UDI-DI variants, MDR

MD Atlas
SCHWIND eye-tech-solutions GmbH

Data from EUDAMED, last updated May 23, 2026

SCHWIND AMARIS

426015714E057-EXCIMER6M

3 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: SCHWIND eye-tech-solutions GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 426015714E057-EXCIMER6M
Device name: SCHWIND AMARIS
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: SCHWIND eye-tech-solutions GmbH
SRN: DE-MF-000019049
Country: Germany
Email: info@eye-tech.net

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KPNEMV5ZVA9C8SEVM5T0MM1N

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

1860004260157140240
1680004260157140219
1850004260157140226